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187039-57-2

187039-57-2 Structure

187039-57-2 Structure
IdentificationBack 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 PropertiesBack 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
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID(187039-57-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

N-(tert-Butoxycarbonyl)-(3S)-hydroxy-L-proline methyl ester

184046-78-4

BOC-(2S,3S)-3-HYDROXYPYRROLIDINE-2-CARBOXYLIC ACID

187039-57-2

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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