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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 57589Generated: October 25, 2026

Ethanol → Ethyl 1-(4-bromophenyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/57589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(4-Bromophenyl)piperidine-4-carboxylic acidHCID 71093671—
ProductEthyl 1-(4-bromophenyl)piperidine-4-carboxylateHCID 71093667—

Reaction Steps

To a stirred solution of 1-(4-bromophenyl)piperidine-4-carboxylic acid (1.56 g, 5.5 mmol) in absolute ethanol (30 mL) was cooled to 0° C. and SOCl2 (1.18 g, 10 mmol) added drop-wise. The mixture was stirred to room temperature and heated to reflux for 3 hours. The reaction mixture was evaporated in vacuo and the residue dissolved in saturated aqueous solution of NaHCO3 (50 mL). The aqueous solution was extracted with EtOAc (3×30 mL). The organic extracts was dried over Na2SO4, filtered and evaporated in vacuo. The residue was purified by silica gel column chromatography (eluent; ethyl acetate: hexane=1:1) to yield the title compound pale brown oil 1.08 g. MS (m/z): 314 (M+2)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434726B2
Source datasetuspto-grants-2016_09
ORD IDord-af667b2eab174f76a867511ce26e2bc7
Source noteuspto-grants-2016_09