(S)-BOC-3-AMINO-2-PYRROLIDINONE
(S)-BOC-3-AMINO-2-PYRROLIDINONE Basic information
- Product Name:
- (S)-BOC-3-AMINO-2-PYRROLIDINONE
- Synonyms:
-
- (S)-BOC-3-AMINO-2-PYRROLIDINONE
- (S)-(-)-3-BOC-AMINOPYRROLIDIN-2-ONE
- CarbaMic acid, N-[(3S)-2-oxo-3-pyrrolidinyl]-, 1,1-diMethylethyl ester
- tert-butyl 2-oxopyrrolidin-3-ylcarbaMate
- (S)-tert-butyl 2-oxopyrrolidin-3-ylcarbaMate
- (2-oxopyrrolidin-3-(S)-yl)carbaMic acid tert-butyl ester
- 2-Methyl-2-propanyl [(3S)-2-oxo-3-pyrrolidinyl]carbaMate
- tert-butyl (S)-(2-oxopyrrolidin-3-yl)carbamate
- CAS:
- 92235-34-2
- MF:
- C9H16N2O3
- MW:
- 200.23
- Product Categories:
-
- pharmacetical
- Amino Acids & Deriv.
- CHIRAL CHEMICALS
- Mol File:
- 92235-34-2.mol
(S)-BOC-3-AMINO-2-PYRROLIDINONE Chemical Properties
- Melting point:
- 168.0-170.3 °C(Solv: ethyl acetate (141-78-6); ligroine (8032-32-4))
- Boiling point:
- 394.0±31.0 °C(Predicted)
- Density
- 1.13±0.1 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 11.05±0.20(Predicted)
- Appearance
- White to off-white Solid
(S)-BOC-3-AMINO-2-PYRROLIDINONE Usage And Synthesis
Synthesis
24424-99-5
4128-00-1
92235-34-2
Step 1: (S)-3-Amino-2-pyrrolidinone (3.1 g, 32 mmol) was dissolved in methanol (130 mL) at room temperature and triethylamine (16 mL) and di-tert-butyl dicarbonate (7.7 g, 35.2 mmol) were added sequentially. The reaction mixture was stirred at room temperature overnight and then heated to reflux for 2 hours. After completion of the reaction, the solvent was removed by concentration under reduced pressure and the residue was purified by column chromatography (eluent: ethyl acetate) to afford (S)-tert-butoxycarbonyl-3-amino-2-pyrrolidinone (5.0 g, 78% yield) as a white solid.
References
[1] Patent: WO2008/33562, 2008, A2. Location in patent: Page/Page column 63
[2] Patent: US2009/76005, 2009, A1. Location in patent: Page/Page column 29; 30
[3] Patent: WO2007/126871, 2007, A1. Location in patent: Page/Page column 61-62
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