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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1074090Generated: October 26, 2026

Ethyl (phenethylthio)acetate → Ethyl 5-dimethylamino-5-phenyl-2-phenethylthio-2,4-pentadienoate

https://huagongshe.com/reaction/1074090

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl (phenethylthio)acetateHCID 304016—
ReactantSodium ethoxideHCID 2723922—
ReactantN-(3-dimethylamino-3-phenylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 75556698—
ReactantEthyl 5-dimethylamino-5-phenyl-2-phenylthio-2,4-pentadienoateHCID 86743587—
SolventEthanolHCID 702—
ProductEthyl 5-dimethylamino-5-phenyl-2-phenethylthio-2,4-pentadienoateHCID 86743602—

Reaction Steps

The procedure is as in Example 24 for the preparation of ethyl 5-dimethylamino-5-phenyl-2-phenylthio-2,4-pentadienoate, starting with N-(3-dimethylamino-3-phenylpropenylidene)-N-methylmethanaminium tetrafluoroborate (5.8 g), a 2M ethanolic solution of sodium ethylate (10 cc) and ethyl (phenethylthio)acetate (4.5 g) in ethanol (50 cc). After purification by chromatography on a silica column with dichloromethane as eluent, ethyl 5-dimethylamino-5-phenyl-2-phenethylthio-2,4-pentadienoate (4.5 g) is obtained in the form of a yellow oil, and is used in the crude state in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04971979
Source datasetuspto-grants-1990_11
ORD IDord-406bcafd387545bfac07e5215afd5620
Source noteuspto-grants-1990_11