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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510195Generated: November 4, 2026

Chloride → HCID 10513182, compound

https://huagongshe.com/reaction/1510195

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
Reactant[1-(4-fluorobenzyl)piperidin-4-yl]methanolHCID 10489280—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10513182HCID 1051318279%

Reaction Steps

A solution of oxylyl chloride (0.59 ml, 3.95 mmol) in CH2Cl2 (20 ml) was cooled to −78° C. DMSO (0.95 ml, 13.38 mmol) was added dropwise into the oxylyl chloride solution. The reaction mixture was stirred for 5 minutes, and 1-[(4-fluorophenyl)methyl]-4-piperidinemethanol (0.99 g, 4.46 mmol) in CH2Cl2 (20 ml) was added dropwise into the reaction solution. Stirring was continued for an additional 20 minutes. Et3N, 8.0 ml was added and the reaction mixture was stirred for 10 minutes and then allowed to warm to room temperature. Water (50 ml) was added and the mixture was extracted with CH2Cl2. The combined CH2Cl2 solution was dried over NaSO4. The evaporation of solvent gave an oil, 0.77 g (79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211916B2
Source datasetuspto-grants-2012_07
ORD IDord-1fe7035f93474f469a53ebd74ce20f89
Source noteuspto-grants-2012_07