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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977292Generated: November 3, 2026

3-Bromocyclohexene → HCID 54357020, compound

https://huagongshe.com/reaction/1977292

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-BromocyclohexeneHCID 137057—
ReactantEthyl 4-(4-hydroxypiperidin-1-yl)benzoateHCID 12717445—
CatalystSilver(II) oxideHCID 92152—
SolventTetrahydrofuranHCID 8028—
ProductHCID 54357020HCID 54357020—

Reaction Steps

A solution of 4-(4-hydroxypiperidin-1-yl)benzoic acid ethyl ester (5.4 g), silver oxide (5.31 g) and 3-bromocyclohexene (3.24 ml) in tetrahydrofuran (52 ml) was stirred for 1 day at room temperature. The reaction mixture was filtered off, and the filtrate was concentrated by evaporation under reduced pressure. To the residue was added ethyl acetate, and the resulting precipitate was collected by filtration and dried. The residue was purified by silica gel chromatography (3:2 hexane-ethyl acetate elution) to give 4-[4-(2-cyclohexenyloxy)piperidin-1-yl]benzoic acid ethyl ester (3.84 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232290B1
Source datasetuspto-grants-2001_05
ORD IDord-d5ffdc885b8449e195c0d3dd38f93a74
Source noteuspto-grants-2001_05