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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390606Generated: October 26, 2026

Sodium hydride → Ethyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrate

https://huagongshe.com/reaction/390606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantEthyl 2-(diethoxyphosphoryl)butanoateHCID 229053—
Reactant3'-Methylaminobiphenyl-4-carbaldehydeHCID 1394524—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-[1-(3'-methylaminobiphenyl-4-yl)meth-(e)-ylidene]butyrateHCID 6896249672%

Reaction Steps

197 mg (4.9 mmol) of sodium hydride are added to a mixture of 1.2 mL (4.9 mmol) of triethyl 2-phosphonobutyrate and 415 mg of 3′-methylaminobiphenyl-4-carbaldehyde (2.0 mmol) in 10 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature overnight, poured into saturated aqueous ammonium chloride solution and extracted with ethyl acetate. The organic phases are combined, washed with water and dried over sodium sulfate. The solvent is evaporated off and the residue (1.1 g) is purified by chromatography on a column of silica eluted with a 90/10 heptane/ethyl acetate mixture. 438 mg (72%) of ethyl 2-[1-(3′-methylaminobiphenyl-4-yl)meth-(E)-ylidene]butyrate are obtained in the form of off-white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-919b2e7b34d54fd6b60e8686154cb1ac
Source noteuspto-grants-2013_02