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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220632Generated: October 26, 2026

Ethyl bromoacetate → Ethyl 4'-ethoxycarbonylmethoxybiphenyl-4-carboxylate

https://huagongshe.com/reaction/2220632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantDiethylamineHCID 8021—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 4'-hydroxy-4-biphenylcarboxylateHCID 4049156—
SolventDimethylformamideHCID 6228—
ProductEthyl 4'-ethoxycarbonylmethoxybiphenyl-4-carboxylateHCID 2313418599.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 4′-hydroxybiphenyl-4-carboxylate (2.262 g), ethyl bromoacetate (1.871 g) and potassium carbonate (1.940 g) in N,N-dimethylformamide (50 mL) was stirred at 60° C. for 1 hr. Diethylamine (6.820 g) was added to the reaction mixture. After being stirred at room temperature for 30 minutes, the mixture was partitioned between ethyl acetate and water. The organic layer was washed successively with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford ethyl 4′-ethoxycarbonylmethoxybiphenyl-4-carboxylate (3.06 g) as a crude product. A mixture of the crude ethyl 4′-ethoxycarbonylmethoxybiphenyl-4-carboxylate, sodium borohydride (0.706 g), tetrahydrofuran (40 mL) and ethanol (10 mL) was stirred at 60° C. for 1 hr. Methanol (10 mL) was added to the reaction mixture, and stirred at room temperature for additional 30 minutes. The solvent was evaporated under reduced pressure, and the residue was partitioned between ethyl acetate and 1 mol/L hydrochloric acid. The organic layer was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to afford the title compound (3.000 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417169B2
Source datasetuspto-grants-2008_08
ORD IDord-a58985a15cdc4d10bfb658cec15182ef
Source noteuspto-grants-2008_08