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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212047Generated: November 1, 2026

Methyl Acrylate → HCID 1474745, compound

https://huagongshe.com/reaction/2212047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Bromophenyl cyclopropyl ketoneHCID 81394—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 1474745HCID 147474547.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (4-bromophenyl)-(cyclopropyl)methanone (0.450 g, 2.00 mmol), palladium acetate 49 mg, 0.220 mmol), triphenylphosphine (55 mg, 0.21 mmol), methyl acrylate (0.43 g, 2.50 mmol) and triethylamine (10 ml, 72 mmol) was heated to 100° C. for 48 in a closed reaction vial. The reaction mixture was cooled to room temperature. The solid was removed by filtration. A mixture of ice and 1 N hydrochloric acid was added to the liquid. The mixture was stirred for 1 h at room temperature. It was extracted with ethyl acetate (2×150 ml). The combined organic layers were washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml) and dried over magnesium sulphate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (40 g) using a mixture of dichloromethane/ethyl acetate/heptane (1:1:1) as eluent, to give 217 mg of (E)-3-(4-(cyclopropanecarbonyl)phenyl)acrylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101898B2
Source datasetuspto-grants-2006_09
ORD IDord-e2aac1089cfd45189cd6646ce92bc719
Source noteuspto-grants-2006_09