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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423943Generated: October 25, 2026

Hydrochloric Acid → Methyl (E)-3-(4'-hydroxy-[1,1'-biphenyl]-4-yl)acrylate

https://huagongshe.com/reaction/423943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl AcrylateHCID 7294—
ReactantEthyl AcetateHCID 8857—
Reactant4-Bromo-4'-hydroxybiphenylHCID 95093—
CatalystTri-o-tolylphosphineHCID 80271—
Catalystpalladium(II) acetateHCID 167845—
SolventTriethylamineHCID 8471—
ProductMethyl (E)-3-(4'-hydroxy-[1,1'-biphenyl]-4-yl)acrylateHCID 994301383.3%

Reaction Steps

A mixture of 2 g (8.03 mmol) of 4-(4-bromophenyl)phenol, 1.1 g (12.8 mmol) of methyl acrylate, 18 mg (0.08 mmol) of Palladium acetate, and 94 mg (0.31 mmol) of tri-(o-tolyl)phosphine in 3.7 ml of triethylamine was refluxed for 6 hours. A further 6 mg of Palladium acetate and 30 mg of tri-(o-tolyl)phosphine were added and heated for an hour, then a further 30 mg of Palladium acetate and 94 mg di tri-(o-toluyl)phosphine were added and heated for 3.5 hours. Then the reaction was acidified with 6M HCl, ethyl acetate was added, and stirred for a time to dissolve the precipitate, the phases were separated, the organic phase dried over Na2SO4 and the solvent evaporated. The crude product (934 mg) was purified by taking up in hexane/ethyl ether and filtered off to give 1.7 g of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101793B2
Source datasetuspto-grants-2012_01
ORD IDord-035780a292874a2e8454a557de2fa9e3
Source noteuspto-grants-2012_01