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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094747Generated: October 25, 2026

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

https://huagongshe.com/reaction/1094747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantCesium carbonateHCID 10796—
ReactantBenzyl (S)-(-)-tetrahydro-5-oxo-3-furanylcarbamateHCID 697922—
SolventWaterHCID 962—
Product(3S)-4-Hydroxy-3-({[(phenylmethyl)oxy]carbonyl}amino)butanoic acidHCID 13340757—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133908B2
Source datasetuspto-grants-2012_03
ORD IDord-e541810d00e048ceb3fa3ad3bc41bdc7
Source noteuspto-grants-2012_03