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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661748Generated: October 31, 2026

Ethanol → HCID 86617335, compound

https://huagongshe.com/reaction/661748

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 numberUS08084644B2
Source datasetuspto-grants-2011_12
ORD IDord-a1f938d760964fd8b184aed082acbadb
Source noteuspto-grants-2011_12