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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267152Generated: October 29, 2026

Ethanol → HCID 54074795, compound

https://huagongshe.com/reaction/267152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 86751127HCID 86751127—
ProductHCID 54074795HCID 54074795—

Reaction Steps

1.02 g of benzyl [3-chloro-2(S)-hydroxypropyl-1(S)-[(2-naphthyl)methyl]propyl]carbamate were stirred in 40 ml of ethanol with 4 ml of 0.7M potassium hydroxide solution in ethanol for 0.75 hours. The solvent was removed by evaporation and the residue was partitioned between dichloromethane and water. The organic phase was dried over anhydrous sodium sulphate and evaporated to give a white solid which was recrystallized from ethyl acetate/n-hexane. There was obtained 0.879 g of 3(S)-(benzyloxyformamido)-1,2(S)-epoxy-4-(2-naphthyl)butane as a white solid of melting point 115°-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652369
Source datasetuspto-grants-1997_07
ORD IDord-db9636b86efe48e984757fcd0c8a5740
Source noteuspto-grants-1997_07