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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 987929Generated: October 30, 2026

Ethyl Acetate → HCID 86759215, compound

https://huagongshe.com/reaction/987929

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant6381-59-5HCID 165453—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 69853659HCID 69853659—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 86759215HCID 86759215—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 4-benzyl-5-ethoxycarbonylmethyl-2,2-dimethyl-oxazolidine-3-carboxylic acid tert-butyl ester (48 g, 0.12 mol) in dry toluene was stirred at −78° C. during the addition of 1M diisobutyl aluminium hydride in toluene (165 ml, 165 mmol). The resulting mixture was stirred at −78° C. for 4 hours and ethyl acetate (60 ml) was then added. After 30 minutes, the mixture was allowed to warm to room temperature and a solution of potassium sodium L-tartrate tetrahydrate (250 g, mmoL) in water (800 ml) was added. The resulting biphasic mixture was stirred until the two phases were clear. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried (anhydrous magnesium sulfate) and concentrated in vacuo to provide 4-benzyl-2,2-dimethyl-(2-oxo-ethyl)-oxazolidine-3-carboxylic acid tert-butyl ester which solidified upon standing overnight.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06632826B1
Source datasetuspto-grants-2003_10
ORD IDord-a8f8b930eaa84e298a3164285e6dce70
Source noteuspto-grants-2003_10