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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1275387Generated: November 2, 2026

Ethyl Acetate → Methyl 3-bromocinnamate, predominantly trans

https://huagongshe.com/reaction/1275387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant3-(3-Bromophenyl)-2-propen-1-olHCID 18676478—
ProductMethyl 3-bromocinnamate, predominantly transHCID 148275173%

Reaction Steps

The title compound was prepared from trans-3-(3-bromophenyl)-2-propenol by a sequence analogous to that described above for compound (9a) but using D-(-)-diethyl tartrate. Column chromatography (ethyl acetate--light petroleum (b.p. 40-60° C.), 3:7) provided the title compound (73%) as a pale yellow oil. Distilled at 160-185° C. at 0.1 mmHg. using a Kugelrohr short path distillation apparatus as a colourless oil; [α]D25 +37.6 (c=0.020 gml-1, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06160120
Source datasetuspto-grants-2000_12
ORD IDord-4d9fef9211844890b29826ee635256d3
Source noteuspto-grants-2000_12