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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889170Generated: October 25, 2026

Piperidine → Bromo-[4-(piperidine-1-sulfonyl)-phenyl]-acetic acid ethyl ester

https://huagongshe.com/reaction/1889170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantBromo-(4-chlorosulfonyl-phenyl)-acetic acid ethyl esterHCID 59610030—
SolventDichloromethaneHCID 6344—
ProductBromo-[4-(piperidine-1-sulfonyl)-phenyl]-acetic acid ethyl esterHCID 5961003953.6%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Bromo-(4-chlorosulfonyl-phenyl)-acetic acid ethyl ester (2.08 gm, 6.38 mmol) was taken in DCM (63 ml) under argon atmosphere and cooled to 0-5° C., piperidine (0.56 ml, 5.74 mmol) was added dropwise to the mixture at 0-5° C. Reaction mixture was then stirred at room temperature for 30 min. Reaction mixture was washed with water followed by brine solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product, which was purified by flash column chromatography over silica gel using 30-50% ethyl acetate in hexane as eluent to give bromo-[4-(piperidine-1-sulfonyl)-phenyl]-acetic acid ethyl ester (1.2 gm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501955B2
Source datasetuspto-grants-2013_08
ORD IDord-e585ae54d88d46c6b6b7e50c8f1f531d
Source noteuspto-grants-2013_08