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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41703Generated: October 29, 2026

Triethylamine → 4-(4-Bromophenyl)-1-(methanesulphonyl)piperidin-4-ol

https://huagongshe.com/reaction/41703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(4-Bromophenyl)-4-hydroxypiperidineHCID 93911—
SolventDichloromethaneHCID 6344—
Product4-(4-Bromophenyl)-1-(methanesulphonyl)piperidin-4-olHCID 18723205—

Reaction Steps

1 g of 4-(4-bromophenyl)piperidin-4-ol is placed in 20 ml of dichloromethane. 0.65 ml of triethylamine and then 0.33 ml of methanesulphonyl chloride are added. The reaction mixture is stirred at ambient temperature for 2 h. It is washed with water and then with a saturated aqueous sodium chloride solution. The organic phase is dried over sodium sulphate and then evaporated under reduced pressure. The crude product obtained is chromatographed on silica gel, elution being carried out with a dichloromethane/methanol (99/1) solvent mixture. 1.1 g of 4-(4-bromophenyl)-1-(methanesulphonyl)piperidin-4-ol are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530657B2
Source datasetuspto-grants-2013_09
ORD IDord-912b160d0d294e57b5d2e395040ec0ab
Source noteuspto-grants-2013_09