ChemicalBook--->CAS DataBase List--->348165-62-8

348165-62-8

348165-62-8 Structure

348165-62-8 Structure
IdentificationBack Directory
[Name]

(2R, 4S)-4-Hydroxy-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester
[CAS]

348165-62-8
[Synonyms]

(2R,4S)-tert-Butyl 4-hydroxy-2-methylpyrrolidine-1-carboxylate
tert-butyl (2R,4S)-4-hydroxy-2-methylpyrrolidine-1-carboxylate
(2R, 4S)-4-Hydroxy-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester
1-Pyrrolidinecarboxylic acid, 4-hydroxy-2-methyl-, 1,1-dimethylethyl ester, (2R,4S)-
[Molecular Formula]

C10H19NO3
[MOL File]

348165-62-8.mol
[Molecular Weight]

201.26
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,2-8°C
[Appearance]

White to off-white Solid
[Optical Rotation]

Consistent with structure
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H317
[Precautionary statements ]

P280
Spectrum DetailBack Directory
[Spectrum Detail]

(2R, 4S)-4-Hydroxy-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester(348165-62-8)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Pyrrolidinecarboxylic acid, 2-methyl-4-[(4-nitrobenzoyl)oxy]-, 1,1-dimethylethyl ester, (2R,4S)-

348165-61-7

(2R, 4S)-4-Hydroxy-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester

348165-62-8

Compound 15 (0.885 g, 2.51 mmol) was dissolved in methanol (5 mL) followed by addition of tetrahydrofuran (5 mL) and 2N sodium hydroxide solution at room temperature. The reaction mixture was stirred for 30 min, poured into water and extracted with ethyl acetate. The organic layers were combined, washed with saturated brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give compound 13 (0.52 g, 100% yield) as a colorless solid.

[References]

[1] Patent: US2007/117986, 2007, A1. Location in patent: Page/Page column 24
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