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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 327941Generated: October 27, 2026

Tetrahydrofuran → 2-[(5-Bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester

https://huagongshe.com/reaction/327941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-[2-[(5-Bromopentyl)oxy]-5-chlorophenyl]-2-propenoic acid methyl esterHCID 53828054—
ReactantHCID 178418361HCID 178418361—
CatalystRhodiumHCID 23948—
SolventTolueneHCID 1140—
Product2-[(5-Bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl esterHCID 54391460100.8%

Reaction Steps

A mixture of 2.02 g (5.59 mmol) of 3-[2-[(5-bromopentyl)oxy]-5-chlorophenyl]-2-propenoic acid methyl ester (mixture of E/Z isomers), 90 mL of tetrahydrofuran, 190 mL of toluene, and 1.26 g of 5% rhodium on alumina was stirred at room temperature, in an atmosphere of hydrogen, until reduction was complete. The catalyst was removed by suction filtration and the filtrate was concentrated in vacuo giving 2.05 g (ca. 100%) of 2-[(5-bromopentyl)oxy]-5-chlorobenzenepropanoic acid methyl ester as a pale-yellow oil which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05273999
Source datasetuspto-grants-1993_12
ORD IDord-7239bf6c1db74d52b599f4d574a48ecf
Source noteuspto-grants-1993_12