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词条 Tert-Butyloxycarbonyl protecting group
释义

  1. Amine protection

      Common amine protection methods    Common amine deprotection methods  

  2. References

{{DISPLAYTITLE:tert-Butyloxycarbonyl protecting group}}

The tert-butyloxycarbonyl protecting group or tert-butoxycarbonyl protecting group[1] (BOC group) is a protecting group used in organic synthesis.

The BOC group can be added to the amine under aqueous conditions using di-tert-butyl dicarbonate in the presence of a base such as sodium bicarbonate:

Protection of the amine can also be accomplished in acetonitrile solution using 4-dimethylaminopyridine (DMAP) as the base.

Removal of the BOC in amino acids can be accomplished with strong acids such as trifluoroacetic acid neat or in dichloromethane, or with HCl in methanol.[2][3][4] A complication may be the tendency of the t-butyl cation intermediate to alkylate other nucleophiles; scavengers such as anisole or thioanisole may be used.[5][6]

Selective cleavage of the N-Boc group in the presence of other protecting groups is possible when using AlCl3.

Sequential treatment with trimethylsilyl iodide then methanol can also be used for Boc deprotection,[7][8] especially where other deprotection methods are too harsh for the substrate.[9] The mechanism involves silylation of the carbonyl oxygen and elimination of tert-butyl iodide ({{EquationNote|1}}), methanolysis of the silyl ester to the carbamic acid ({{EquationNote|2}}) and finally decarboxylation to the amine ({{EquationNote|3}}).[10]

{{NumBlk|:|R2NCO2tBu + Me3SiI → R2NCO2SiMe3 + tBuI|{{EquationRef|1}}}}{{NumBlk|:|R2NCO2SiMe3 + MeOH → R2NCO2H + MeOSiMe3|{{EquationRef|2}}}}{{NumBlk|:|R2NCO2H → R2NH + CO2|{{EquationRef|3}}}}

Amine protection

The tert-butyloxycarbonyl (Boc) group is used as a protecting group for amines in organic synthesis.

Common amine protection methods

  • Simple rapid stirring of a mixture of the amine and di-tert-butyl dicarbonate (Boc2O) suspended in water at ambient temperature, an example of an on-water reaction.[11]
  • Heating a mixture of the amine to be protected and di-tert-butyl dicarbonate in tetrahydrofuran (THF) at 40 °C[12]
  • Add the amine to sodium hydroxide and di-tert-butyl dicarbonate in water and THF at 0 °C then warm to ambient temperature.[13]
  • Heating a mixture of the amine to be protected and di-tert-butyl dicarbonate in a biphasic mixture of chloroform and aqueous sodium bicarbonate at reflux for 90 minutes.[14]
  • Add the amine to di-tert-butyl dicarbonate, 4-dimethylaminopyridine (DMAP), and acetonitrile (MeCN) at ambient temperature[15]

BOC-protected amines are prepared using the reagent di-tert-butyl-iminodicarboxylate. Upon deprotonation, this reagent affords a doubly BOC-protected source of NH{{su|b=2|p=−}}, which can be N-alkylated. The approach is complementary to the Gabriel synthesis of amines.

Common amine deprotection methods

  • Mix the protected carbamate to be deprotected with 3 M hydrochloric acid (HCl) in ethyl acetate for 30 min at ambient temperature[16]
  • Heat the carbamate in a mixture of aqueous hydrochloric acid and toluene at 65 °C[17]
  • Dissolving desired protected compound in a 50/50 mix of dichloromethane and trifluoroacetic acid [18]

References

1. ^{{Cite web|url=http://iupac.org/publications/pac/pdf/2013/pdf/8501x0307.pdf|title=Rules for abbreviation of protecting groups|last=|first=|date=2013|website=IUPAC|publisher=iupac.org|pages=|type=|archive-url=|archive-date=|dead-url=|access-date=}}
2. ^{{OrgSynth | author1 = Robert M. Williams | author2 = Peter J. Sinclair | author3 = Duane E. DeMong | author4 = Daimo Chen | author5 = Dongguan Zhai | prep = v80p0018 | title = Asymmetric Synthesis of N-tert-Butoxycarbonyl α-Amino Acids. Synthesis of (5S,6R)-4-tert-Butoxycarbonyl-5,6-diphenylmorpholin-2-one (4-Morpholinecarboxylic acid, 6-oxo-2,3-diphenyl-, 1,1-dimethylethyl ester, (2S,3R)-)]| volume = 80 | pages = 18 | year = 2003 | doi = 10.15227/orgsyn.080.0018}}
3. ^{{cite journal |author1=E. A. Englund |author2=H. N. Gopi |author3=D. H. Appella | title = An Efficient Synthesis of a Probe for Protein Function: 2,3-Diaminopropionic Acid with Orthogonal Protecting Groups | journal = Org. Lett. | year = 2004 | volume = 6 | pages = 213–215 | doi = 10.1021/ol0361599 | pmid = 14723531 | issue = 2}}
4. ^{{cite journal |author1=D. M. Shendage |author2=R. Fröhlich |author3=G. Haufe | title = Highly Efficient Stereoconservative Amidation and Deamidation of α-Amino Acids | journal = Org. Lett. | year = 2004 | volume = 6 | pages = 3675–3678 | doi = 10.1021/ol048771l | pmid = 15469321 | issue = 21}}
5. ^{{cite journal | doi = 10.1111/j.1399-3011.1978.tb02896.x | title = Removal of t-Butyl and t-Butoxycarbonyl Protecting Groups with Trifluoroacetic acid | year = 1978 | last1 = Lundt | first1 = Behrend F. | last2 = Johansen | first2 = Nils L. | last3 = Vølund | first3 = Aage | last4 = Markussen | first4 = Jan | journal = Int. J. Pept. Protein Res. | volume = 12 | issue = 5 | pages = 258–268 | pmid = 744685}}
6. ^{{cite book | doi = 10.1002/9783527631827.ch1 | chapter = Protection Reactions | editor = Andrew B. Hughes | author1 = Vommina V. Sureshbabu | author2 = Narasimhamurthy Narendra | volume = 4 | series = Amino Acids, Peptides and Proteins in Organic Chemistry | title = Protection Reactions, Medicinal Chemistry, Combinatorial Synthesis | publisher = Wiley-VCH | chapter-url = https://books.google.com.au/books?id=uZK2i-FkeAUC&pg=PP18 | isbn = 9783527641574 | pages = XVIII – LXXXIV| year = 2011 }}
7. ^{{ cite journal |author1=Richard S. Lott |author2=Virander S. Chauhan |author3=Charles H. Stammer | title = Trimethylsilyl iodide as a peptide deblocking agent | journal = J. Chem. Soc., Chem. Commun. |issue=11 | year = 1979 | pages = 495–496 | doi = 10.1039/C39790000495 }}
8. ^{{ cite journal | doi = 10.1016/0040-4020(82)87002-6 | title= Iodotrimethylsilane—a versatile synthetic reagent| year = 1982 | last1 = Olah | first1 = G | last2 = Narang | first2 = S. C. | journal = Tetrahedron | volume = 38 | issue = 15 | pages = 2225–2277 }}
9. ^{{ cite journal |author1=Zhijian Liu |author2=Nobuyoshi Yasuda |author3=Michael Simeone |author4=Robert A. Reamer | title = N-Boc Deprotection and Isolation Method for Water-Soluble Zwitterionic Compounds | journal = J. Org. Chem. | year = 2014 | volume = 79 |issue=23 | pages = 11792–11796 | doi = 10.1021/jo502319z |pmid=25376704 }}
10. ^{{ cite journal |author1=Michael E. Jung |author2=Mark A. Lyster | title = Conversion of alkyl carbamates into amines via treatment with trimethylsilyl iodide | journal = J. Chem. Soc., Chem. Commun. |issue=7 | year = 1978 | pages = 315–316 | doi = 10.1039/C39780000315 }}
11. ^{{Cite journal|last=Chankeshwara|first=Sunay V.|last2=Chakraborti|first2=Asit K.|year=2006|title=Catalyst-Free Chemoselective N-tert-Butyloxycarbonylation of Amines in Water|doi=10.1021/ol0611191|pmid=16836380|journal=Org. Lett.|volume=8|issue=15|pages=3259–3262}}
12. ^{{Cite book|chapter-url=http://onlinelibrary.wiley.com/book/10.1002/0470053488|title=Greene's Protective Groups in Organic Synthesis|edition = 4th|publisher = John Wiley & Sons|last=Wuts|first=Peter G. M.|last2=Greene|first2=Theodora W.|doi=10.1002/9780470053485.ch7|isbn=9780471697541|chapter=Protection for the Amino Group|pages=696–926|year=2006}}
13. ^{{cite journal|author1 = Fachao Yan|author2 = Hanbing Liang|author3 = Jian Song|author4 = Jie Cui|author5 = Qing Liu|author6 = Sheng Liu|author7 = Ping Wang|author8 = Yunhui Dong|author9 = Hui Liu|title = Palladium-Catalyzed Cyclization-Heck Reaction of Allenamides: An Approach to 3-Methylene-5-phenyl-1,2,3,4-tetrahydropyridine Derivatives|journal = Org. Lett.|year = 2017|volume = 19|issue = 1|pages = 86–89|doi = 10.1021/acs.orglett.6b03364|pmid = 27966983}}
14. ^{{Cite journal|last=Tarbell|first=D. Stanley|last2=Yamamoto|first2=Yutaka|last3=Pope|first3=Barry M.|year=1972|title=New Method to Prepare N-t-Butoxycarbonyl Derivatives and the Corresponding Sulfur Analogs from di-t-Butyl Dicarbonate or di-t-Butyl Dithiol Dicarbonates and Amino Acids|journal=Proc. Natl. Acad. Sci. U.S.A.|volume=69|issue=3|pages=730–732|pmc=426545|pmid=16591972|doi=10.1073/pnas.69.3.730|bibcode=1972PNAS...69..730T}}
15. ^{{Cite journal|last=Englund|first=Ethan A.|last2=Gopi|first2=Hosahudya N.|last3=Appella|first3=Daniel H.|title=An Efficient Synthesis of a Probe for Protein Function: 2,3-Diaminopropionic Acid with Orthogonal Protecting Groups|journal=Org. Lett.|volume=6|issue=2|pages=213–215|doi=10.1021/ol0361599|pmid=14723531|year=2004}}
16. ^{{Cite journal|last=Stahl|first=Glenn L.|last2=Walter|first2=Roderich|last3=Smith|first3=Clark W.|title=General Procedure for the Synthesis of Mono-N-Acylated 1,6-Diaminohexanes|journal=J. Org. Chem.|volume=43|issue=11|pages=2285–2286|doi=10.1021/jo00405a045|year=1978}}
17. ^{{Cite journal|last=Prashad|first=Mahavir|last2=Har|first2=Denis|last3=Hu|first3=Bin|last4=Kim|first4=Hong-Yong|last5=Girgis|first5=Michael J.|last6=Chaudhary|first6=Apurva|last7=Repič|first7=Oljan|last8=Blacklock|first8=Thomas J.|last9=Marterer|first9=Wolfgang|title=Process Development of a Large-Scale Synthesis of TKA731: A Tachykinin Receptor Antagonist|journal=Org. Process Res. Dev.|volume=8|issue=3|pages=330–340|doi=10.1021/op0341824|year=2004}}
18. ^{{Cite web | url=http://commonorganicchemistry.com/Rxn_Pages/Boc_Protection/Boc_Protection_TFA.htm | title=Boc Deprotection - TFA}}
{{DEFAULTSORT:Butyloxycarbonyl protecting group, tert-}}

2 : Protecting groups|Tert-butyl compounds
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