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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757007Generated: November 1, 2026

Triethylamine → 1-(4-Cyanophenyl)-4-mesyloxymethyl-piperidine

https://huagongshe.com/reaction/1757007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(4-(Hydroxymethyl)piperidin-1-yl)benzonitrileHCID 19391296—
SolventDichloromethaneHCID 6344—
Product1-(4-Cyanophenyl)-4-mesyloxymethyl-piperidineHCID 19391270—

Reaction Steps

To a solution of 5.5 g of 1-(4-cyanophenyl)-4-hydroxymethyl-piperidine and 5.16 g of triethylamine in 150 ml of methylene chloride, 5.84 g of methanesulphonic acid chloride are slowly added dropwise at ambient temperature and with stirring. After it has all been added the mixture is left to stand overnight and the solvent is removed under reduced pressure. The residue is chromatographed with methylene chloride/methanol (50:1) over silica gel. Yield: 6.95 g (93% of theory), Mass spectrum: (M+H)+ =295

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05442064
Source datasetuspto-grants-1995_08
ORD IDord-70d7912ec63f40edb04c7797831045c4
Source noteuspto-grants-1995_08