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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477353Generated: October 30, 2026

Ethanol → HCID 54557924, compound

https://huagongshe.com/reaction/477353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium ethoxideHCID 2723922—
ReactantEthyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino2,4-hexadienoateHCID 44325574—
ReactantN-(dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborateHCID 86743575—
ProductHCID 54557924HCID 54557924—

Reaction Steps

The procedure is as in Example 4 for the preparation of ethyl 6-phenyl-6-oxo-5-methylthio-2-dimethylamino-2,4-hexadienoate, starting with N-(3-dimethylamino-3-ethoxycarbonylpropenylidene)-N-methylmethanaminium tetrafluoroborate (8 g), a 2M ethanolic solution of sodium ethylate (14 cc) and ethyl 1-(3-biphenylyl)acetate (6.7 g) in ethanol (30 cc). After purification by chromatography on a silica column with dichloromethane as eluent, diethyl 2-dimethylamino-5-(3-biphenylyl)-2,4-hexadienedioate (4.2 g) is obtained in the form of a yellow oil, and is used in the curde state in the subsequent syntheses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886835
Source datasetuspto-grants-1989_12
ORD IDord-b1614d6b443c453bb3e0d50f38ad1fc0
Source noteuspto-grants-1989_12