Identification | Back Directory | [Name]
BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID | [CAS]
187039-57-2 | [Synonyms]
BOC-TRANS-3-HYDROXY-L-PROLINE BOC-(2S,3S)-3-HYDROXY-2-PYRROLIDINECARBOXYLIC ACID BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID (2S,3S)-1-(TERT-BUTOXYCARBONYL)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID (2S,3S)-3-Hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester ( 2S, 3S)-3-hydroxy-pyrrolidine-1,2-dicarboxylic acid tert butyl ester (2S,3S)-3-Hydroxy-1,2-pyrrolidinedicarboxylic acid 1-(1,1-dimethylethyl) ester 1,2-Pyrrolidinedicarboxylicacid, 3-hydroxy-, 1-(1,1-diMethylethyl) ester, (2S,3S)- (2S,3S)-3-hydroxy-1-[(2-methylpropan-2-yl)oxycarbonyl]pyrrolidine-2-carboxylic acid PRODUCT ENGLISH NAME: (2S,3S)-1-(TERT-BUTOXYCARBONYL)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID | [Molecular Formula]
C10H17NO5 | [MDL Number]
MFCD04974546 | [MOL File]
187039-57-2.mol | [Molecular Weight]
231.25 |
Chemical Properties | Back Directory | [Melting point ]
157℃ | [Boiling point ]
390.9±42.0 °C(Predicted) | [density ]
1.312±0.06 g/cm3 (20 ºC 760 Torr) | [storage temp. ]
2-8°C | [pka]
3.69±0.40(Predicted) | [Appearance]
White to light brown Solid |
Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of N-Boc-(2S,3S)-(2S,3S)-3-hydroxy-2-carboxypyrrolidine from (2S,3S)-1-(tert-butoxycarbonyl)-3-hydroxy-pyrrolidine-2-carboxylic acid methyl ester: to 1-(tert-butoxycarbonyl)-2-methyl-(2S,3S)-3-hydroxypyrrolidine-1,2-dicarboxylate (0.30 g, 1.22 mmol) in a tetrahydrofuran (12 mL) solution was added to 0.2N aqueous lithium hydroxide (6.12 mL, 1.22 mmol). The reaction mixture was stirred at room temperature for 3 hours. After the reaction was completed, the reaction mixture was diluted with ether (30 mL) and extracted with 0.2N aqueous lithium hydroxide solution (3 x 5 mL). The aqueous layers were combined and acidified with 5% aqueous hydrochloric acid to pH=2. The acidic aqueous layer was extracted with ethyl acetate (3 x 30 mL). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated in vacuum to afford N-Boc-(2S,3S)-3-hydroxy-2-carboxypyrrolidine as a gel (0.25 g, 88% yield), which was used directly in the next reaction. Mass spectrum (ES+) m/z 230.3 (M+1). | [References]
[1] Patent: WO2016/7534, 2016, A1. Location in patent: Page/Page column 171; 172 |
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