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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616342Generated: October 26, 2026

4-Toluenesulfonyl chloride → 4-Bromo-1-tosylpiperidine

https://huagongshe.com/reaction/1616342

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-BromopiperidineHCID 420929—
SolventHydrochloric AcidHCID 313—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product4-Bromo-1-tosylpiperidineHCID 11359032—

Reaction Steps

4-Bromopiperidine (5.75 g, 23.5 mmol) was dissolved in pyridine (50 mL) and treated with tosyl chloride (5.8 g, 30.5 mmol). The reaction mixture was stirred for 12 h at r.t. and then diluted with dichloromethane (150 mL) and HCl (1 M aqueous solution, 50 mL). The organic layer was washed with brine (80 mL), dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (40% EtOAc/hexane) to give 4-bromo-1-tosylpiperidine as a white solid: 1H NMR (400 MHz, CDCl3) δ 7.66 (d, J=8.2 Hz, 2H), 7.34 (d, J=8.2 Hz, 2H), 4.27-4.24 (m, 1H), 3.20-3.17 (m, 2H), 3.13-3.11 (m, 2H), 2.46 (s, 3H), 2.23-2.17 (m, 2H), 2.08-2.05 (m, 2H); MS (ESI) 318.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765788B2
Source datasetuspto-grants-2014_07
ORD IDord-b18ca18d8e344a2d89ea0b4148b50060
Source noteuspto-grants-2014_07