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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024902Generated: October 29, 2026

Ethyl Acetate → (2S,3R)-3-(Benzyloxy)-2-hydroxybutanoic acid

https://huagongshe.com/reaction/1024902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium HydroxideHCID 14798—
ReactantO-BENZYL-L-THREONINEHCID 6951054—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
SolventSulfuric AcidHCID 1118—
Product(2S,3R)-3-(Benzyloxy)-2-hydroxybutanoic acidHCID 67051262—

Reaction Conditions

Temperature-5 °C

Reaction Steps

To a solution of (2S,3R)-2-amino-3-benzyloxy-butyric acid (1.1 g) in 2M sulfuric acid (6.31 mL) was added dropwise over 2 h a solution of sodium nitrite (0.65 g) in water (6 mL), keeping the internal temperature of the reaction below 0° C. The reaction mixture was stirred at −5° C. for 6 h then allowed to warm to room temperature overnight. The mixture was adjusted to pH 4 with 50% aqueous sodium hydroxide then ethyl acetate was added. The mixture was stirred vigorously and acidified to pH 2 with concentrated sulfuric acid. The layers were separated and the aqueous layer extracted with further ethyl acetate (×2). The combined organic extracts were washed with saturated aqueous sodium chloride, dried (MgSO4), filtered and evaporated to give the subtitle compound as a yellow crystalline solid which was used without further purification. Yield: 0.84 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722883B2
Source datasetuspto-grants-2014_05
ORD IDord-480cd663eec74dc2a0b06b834fad68c8
Source noteuspto-grants-2014_05