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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390605Generated: October 26, 2026

Sodium hydride → Ethyl 2-fluoro-3-(3'-methylaminobiphenyl-4-yl)acrylate

https://huagongshe.com/reaction/390605

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3'-Methylaminobiphenyl-4-carbaldehydeHCID 1394524—
ReactantTriethyl 2-fluoro-2-phosphonoacetateHCID 2734865—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 2-fluoro-3-(3'-methylaminobiphenyl-4-yl)acrylateHCID 6895853582.3%

Reaction Steps

382 mg (9.5 mmol) of sodium hydride are added to a solution of 1.9 mL (9.5 mmol) of commercial triethyl 2-fluoro-2-phosphonoacetate in 10 mL of tetrahydrofuran. The reaction mixture is stirred at room temperature for 40 minutes. A solution of 803 mg of 3′-methylaminobiphenyl-4-carbaldehyde prepared as described in Example 5b (3.8 mmol) in 8 mL of tetrahydrofuran is then added dropwise. The reaction mixture is stirred at room temperature overnight. The reaction medium is poured into saturated 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 (2.2 g) is purified by chromatography on a column of silica eluted with an 85/15 heptane/ethyl acetate mixture. 936 mg (82%) of ethyl 2-fluoro-3-(3′-methylaminobiphenyl-4-yl)acrylate are obtained in the form of a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-b4ae4edf07e84bb28529766b5c896665
Source noteuspto-grants-2013_02