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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390603Generated: October 26, 2026

Tetrahydrofuran → Ethyl 2-methyl-3-(3'-methylaminobiphenyl-4-yl)acrylate

https://huagongshe.com/reaction/390603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantEthyl AcetateHCID 8857—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3'-Methylaminobiphenyl-4-carbaldehydeHCID 1394524—
ProductEthyl 2-methyl-3-(3'-methylaminobiphenyl-4-yl)acrylateHCID 6895715567%

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C., a solution of 1.6 mL (9.5 mmol) of triethyl phosphonopropionate in 5 mL of tetrahydrofuran is added to a suspension of 379 mg (9.5 mmol) of sodium hydride in 5 mL of tetrahydrofuran. The mixture is stirred for 15 minutes at 0° C. and a solution of 800 mg (3.8 mmol) of 3′-methylaminobiphenyl-4-carbaldehyde in 5 mL of tetrahydrofuran is then added. The reaction mixture is stirred for 12 hours at room temperature. The reaction is worked up by addition of 50 mL of saturated ammonium chloride solution and extraction with ethyl acetate. The organic phases are washed with sodium chloride solution and dried over magnesium sulfate. The solvents are evaporated off, and the residue is then purified by chromatography on a column of silica eluted with a 7/3 heptane/ethyl acetate mixture. 750 mg (67%) of ethyl 2-methyl-3-(3′-methylaminobiphenyl-4-yl)acrylate, (E) isomer, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383652B2
Source datasetuspto-grants-2013_02
ORD IDord-77a06f07f7184a9987aa881ba6f64cfc
Source noteuspto-grants-2013_02