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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734224Generated: October 26, 2026

Water → Ethyl 3-{1-(4-bromobenzoyl)-4-hydroxypiperidin-4-yl}alpha,alpha-dimethylphenoxyacetate

https://huagongshe.com/reaction/1734224

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantPropanoic acid, 2-bromo-2-methyl-, ethyl esterHCID 11745—
Reactant1-(4-Bromobenzoyl)-4-(2-hydroxyphenyl)-4-hydroxypiperidineHCID 15294673—
ProductEthyl 3-{1-(4-bromobenzoyl)-4-hydroxypiperidin-4-yl}alpha,alpha-dimethylphenoxyacetateHCID 2239936486.4%

Reaction Steps

801 mg of {1-(4-bromobenzoyl)-4-(2-hydroxyphenyl)-4-hydroxypiperidine was stirred for 9 hours at the ambient temperature of 100° C. in the presence of 1.20 g (8.68 mmol) of potassium carbonate in 4.00 g (20.5 ml) of ethyl α-bromoisobutyrate. After completion of the reaction, The reaction mixture was cooled, and water was added thereto, followed by extraction with chloroform. Subsequently, the extract was dried over anhydrous sodium sulfate. Chloroform and the remained ethyl α-bromoisobutyrate was distilled off under reduced pressure to obtain 902 mg (86.4%) of ethyl 3-{1-(4-bromobenzoyl)-4-hydroxypiperidin-4-yl}α,α-dimethylphenoxyacetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532371
Source datasetuspto-grants-1996_07
ORD IDord-1b13c5df5249460cb75e8a2f2a1eeae2
Source noteuspto-grants-1996_07