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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960214Generated: November 3, 2026

Ethanol → HCID 86617335, compound

https://huagongshe.com/reaction/1960214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThiophenolHCID 7969—
ReactantSodiumHCID 5360545—
ReactantN-benzyloxy-3-(phenylthio)acrylimidoyl bromideHCID 86617336—
SolventChloroformHCID 6212—
ProductHCID 86617335HCID 8661733543%

Reaction Steps

Sodium salt of thiophenol (0.14 g) was added to ethanol (5 ml) solution of N-benzyloxy-3-phenylthioacrylimidoyl bromide (0.30 g) at room temperature, then it was heat refluxing for three hours. It was cooled, and chloroform (50 ml) was added to the reaction mixture. It was successively washed with 1N aqueous sodium hydroxide solution, pure water, aqueous saturated sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=20:1) to obtain phenyl N-benzyloxy-3-(phenylthio)thioacrylimidate (0.14 g) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410316B2
Source datasetuspto-grants-2013_04
ORD IDord-14aeb4de498f493fa025b82da578e928
Source noteuspto-grants-2013_04