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5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester

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5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester Basic information
Product Name:5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester
Synonyms:5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester;(S)-tert-Butyl 5-broMo-2-((tert-butoxycarbonyl)aMino)pentanoate;L-Norvaline, 5-bromo-N-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester;ert-butyl(2S)-5-bromo-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoate;5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester USP/EP/BP;tert-butyl (2S)-5-bromo-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoate;N-Boc-5-bromo-L-norvaline tert-butyl ester;tert-butyl (S)-5-bromo-2-((tert-butoxycarbonyl)amino)pentanoate
CAS:91229-86-6
MF:C14H26BrNO4
MW:352.26
EINECS:
Product Categories:
Mol File:91229-86-6.mol
5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester Structure
5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester Chemical Properties
Boiling point 402.7±40.0 °C(Predicted)
density 1.218
storage temp. 2-8°C
pka11.05±0.46(Predicted)
AppearanceWhite to off-white Solid
Safety Information
MSDS Information
5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester Usage And Synthesis
Synthesis
(S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate

90194-99-3

5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester

91229-86-6

The general procedure for the synthesis of tert-butyl (S)-5-bromo-2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate from (S)-2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoic acid is as follows: 1. tert-Butyl (S)-2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate (210.2 mg) was dissolved in dichloromethane (7.3 mL) and cooled to 0°C. 2. Carbon tetrabromide (1.5 eq.) and triphenylphosphine (2.0 eq.) were added sequentially and the reaction mixture was stirred at 0 °C for 20 min. 3. Upon completion of the reaction, the reaction was terminated with hexane/ethyl acetate (2:1, v/v). 4. The reaction mixture was purified by silica gel column chromatography (eluent: hexane/ethyl acetate, 2:1, v/v) to afford 254.6 mg (S)-tert-butyl 5-bromo-2-((tert-butoxycarbonyl)amino)pentanoate in 100% yield as a colorless oil.

References[1] Patent: EP2952504, 2015, A1. Location in patent: Paragraph 0151-0152
[2] European Journal of Organic Chemistry, 2004, # 21, p. 4391 - 4396
[3] Journal of Organic Chemistry, 1984, vol. 49, # 19, p. 3527 - 3534
[4] Chemistry Letters, 1996, # 8, p. 621 - 622
5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester Preparation Products And Raw materials
Raw materials(S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate-->Triphenylphosphine-->Dichloromethane-->Carbon tetrabromide
Tag:5-Bromo-N-[(tert-butoxy)carbonyl]-L-norvaline tert-butyl ester(91229-86-6) Related Product Information
Boc-Asp(OAll)-OH Boc-L-glutamic acid γ-allyl ester (S)-N-Boc-5-Iodo-Nor-OMe (2R)-4-Bromo-2-[[(tert-butoxy)carbonyl]amino]butanoic acid tert-butyl ester (S)-tert-butyl 2-((tert-butoxycarbonyl)amino)-5-hydroxypentanoate D-Norvaline, 5-bromo-N-[(1,1-dimethylethoxy)carbonyl]-, 1,1-dimethylethyl ester