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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477354Generated: October 25, 2026

Sodium ethoxide → Diethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioate

https://huagongshe.com/reaction/477354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl (2-methylbenzylthio)acetateHCID 13245059—
ReactantN-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
ReactantDiethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioateHCID 86743580—
SolventEthanolHCID 702—
ProductDiethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioateHCID 5372038672%

Reaction Steps

The procedure is as in Example 2 for the preparation of diethyl 2-dimethylamino-5-phenylthio-2,4-hexadienedioate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (10 g), a 2M ethanolic solution of sodium ethylate (21 cc) and ethyl (2-methylbenzylthio)acetate (7.9 g) in ethanol (100 cc). After purification by chromatography on a silica column with a mixture of cyclohexane and ethyl acetate (70:30 by volume) as eluent, diethyl 2-dimethylamino-5-(2-methylbenzylthio)-2,4-hexadienedioate (9.5 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 numberUS04886835
Source datasetuspto-grants-1989_12
ORD IDord-e6a5bd963247488d9dd60f39fd7d5c11
Source noteuspto-grants-1989_12