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HRID 1094747생성일: 2026년 10월 26일

Acetone → (3S)-4-Hydroxy-3-({[(phenylmethyl)oxy]carbonyl}amino)butanoic acid

https://huagongshe.com/reaction/1094747

반응식

참여 물질

역할이름HCID투입량
반응물AcetoneHCID 180—
반응물Cesium carbonateHCID 10796—
반응물Benzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamateHCID 697922—
용매WaterHCID 962—
생성물(3S)-4-Hydroxy-3-({[(phenylmethyl)oxy]carbonyl}amino)butanoic acidHCID 13340757—

반응 단계

In a 500 ml round-bottomed flask phenylmethyl [(3S)-5-oxotetrahydro-3-furanyl]carbamate (4.3 g, 18.28 mmol, available from Sigma-Aldrich # 419249) was dissolved in water (100 ml) and acetone (100 ml) and to this solution Cs2CO3 (10.72 g, 32.9 mmol) was added and the reaction left under stirring at room temperature for 5 hours. The solution was then transferred into a separatory funnel and washed with EtOAc (2×50 ml). The aqueous phase was then acidified to pH=2 by the addition of a 2 M HCl aqueous solution and then extracted with EtOAc (5×100 mls). The organic phase was dried (Na2SO4) and solvent removed under reduced pressure to give the title compound D1 (3.78 g) as a white solid. MS: (ES/+) m/z: 254 (M+1). C12H15NO5 requires 253. 1H NMR (400 MHz, DMSO-d6) δ (ppm): 12.11 (bs, 1 H), 7.41-7.07 (m, 5 H), 5.17-4.92 (m, 2 H), 3.95-3.62 (m, 1 H), 3.42-3.22 (m, 2H), 2.55-2.40 (m, 1 H), 2.34-2.23 (m, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08133908B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-e541810d00e048ceb3fa3ad3bc41bdc7
출처 메모uspto-grants-2012_03