tert-Butyl but-3-yn-1-ylcarbamate
tert-Butyl but-3-yn-1-ylcarbamate Basic information
- Product Name:
- tert-Butyl but-3-yn-1-ylcarbamate
- Synonyms:
-
- Carbamic acid, 3-butynyl-, 1,1-dimethylethyl ester (9CI)
- Tert-Butylbut-3-ynylcarbamate
- CarbaMic acid, N-3-butyn-1-yl-, 1,1-diMethylethyl ester
- But-3-ynyl-carbaMic acid tert-butyl ester
- N-BOC-BUT-3YN-1-YLAMINE
- tert-Butyl but-3-yn-1-ylcarbaMate
- tert-butyl N-but-3-ynylcarbamate
- Tert-Butyl But-3-Yn-1-Ylcarbamate(WXC01948)
- CAS:
- 149990-27-2
- MF:
- C9H15NO2
- MW:
- 169.22
- Product Categories:
-
- N-BOC
- Mol File:
- 149990-27-2.mol
tert-Butyl but-3-yn-1-ylcarbamate Chemical Properties
- Boiling point:
- 250.5±23.0 °C(Predicted)
- Density
- 0.976±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 12.11±0.46(Predicted)
- Appearance
- Colorless to light yellow Liquid
tert-Butyl but-3-yn-1-ylcarbamate Usage And Synthesis
Synthesis
6089-09-4
75-65-0
149990-27-2
General procedure for the synthesis of N-Boc-butyn-4-amine from 4-pentynoic acid and tert-butanol: To a solution of 4-pentynoic acid (1.96 g, 20 mmol) in tert-butanol (6 mL) was added triethylamine (3 mL) at 0 °C, followed by the slow addition of diphenylphosphoryl azide (note: the reaction will start rapidly and may proceed violently after addition). The reaction mixture was heated to 85 °C and kept overnight under nitrogen protection. Upon completion of the reaction, the solvent was removed by vacuum concentration and the crude product was purified by silica gel column chromatography using dichloromethane as eluent to give N-Boc-butyn-4-amine as a white solid (1.81 g, 53% yield).
References
[1] Patent: WO2007/28131, 2007, A1. Location in patent: Page/Page column 49
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tert-Butyl but-3-yn-1-ylcarbamate(149990-27-2)Related Product Information
- Carbamic acid, 5-hexynyl-, 1,1-dimethylethyl ester (9CI)
- 2-HYDROXY-3-BUTYNOIC ACID
- tert-Butyl but-3-yn-1-ylcarbamate
- N-DESMETHYLCARBOXY TERBINAFINE
- 2,2-DIMETHYL-BUT-3-YNOIC ACID BENZYL ESTER
- CARBOXYTERBINAFINE
- 3-ETHYNYL-BENZONITRILE
- 2,2-DIMETHYL-BUT-3-YNOIC ACID
- 2-HYDROXY-4-(TRIMETHYLSILYL)-3-BUTYNOIC ACID ETHYL ESTER
- 2-HYDROXY-3-BUTYNOIC ACID ETHYL ESTER
- METHYL 2-AMINO-2-(TRIFLUOROMETHYL)BUT-3-YNOATE
- 3-Quinuclidyl phenyl(3-methyl-1-pentynyl)glycolate A
- 1-Methyl-4-piperidyl phenyl(3-methyl-1-pentynyl)glycolate
- 1-Cyclopenteneglycolic acid, alpha-(1-propynyl)-, 3-quinuclidinyl este r
- AURORA KA-6392
- 1-Methyl-4-piperidyl cyclobutyl(1-propynyl)glycolate
- METHYL 2-(ALLYL[(BENZYLOXY)CARBONYL]AMINO)-2-(TRIFLUOROMETHYL)BUT-3-YNOATE
- METHYL 2-[(TERT-BUTOXYCARBONYL)AMINO]-2-(TRIFLUOROMETHYL)BUT-3-YNOATE