| Identification | Back Directory | [Name]
(S)-BOC-3-AMINO-2-PYRROLIDINONE | [CAS]
92235-34-2 | [Synonyms]
(S)-BOC-3-AMINO-2-PYRROLIDINONE (S)-3-(Boc-amino)-2-pyrrolidone (S)-(-)-3-BOC-AMINOPYRROLIDIN-2-ONE tert-butyl 2-oxopyrrolidin-3-ylcarbaMate (S)-BOC-3-AMINO-2-PYRROLIDINONE USP/EP/BP (S)-tert-butyl 2-oxopyrrolidin-3-ylcarbaMate tert-butyl (S)-(2-oxopyrrolidin-3-yl)carbamate ert-butylN-[(3S)-2-oxopyrrolidin-3-yl]carbamate tert-butyl N-[(3S)-2-oxopyrrolidin-3-yl]carbamate (2-oxopyrrolidin-3-(S)-yl)carbaMic acid tert-butyl ester 2-Methyl-2-propanyl [(3S)-2-oxo-3-pyrrolidinyl]carbaMate CarbaMic acid, N-[(3S)-2-oxo-3-pyrrolidinyl]-, 1,1-diMethylethyl ester | [Molecular Formula]
C9H16N2O3 | [MDL Number]
MFCD03426144 | [MOL File]
92235-34-2.mol | [Molecular Weight]
200.23 |
| Chemical Properties | Back Directory | [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 |
| Hazard Information | Back Directory | [Synthesis]
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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