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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864861Generated: November 2, 2026

Triethylamine → HCID 86638743, compound

https://huagongshe.com/reaction/864861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantPhenylmethyl 4-(1-hydroxyethyl)-1-piperidinecarboxylateHCID 18918437—
SolventDichloromethaneHCID 6344—
ProductHCID 86638743HCID 86638743—

Reaction Steps

A solution of methanesulphonyl chloride (0.85 ml) in dichloromethane (20 ml) was added dropwise to a stirred, ice-cooled solution of triethylamine (1.55 ml) and the product of step (i) (2.64 g) in dichloromethane (50 ml). After stirring for 3 hours the reaction mixture was washed with water (3x) and brine, dried (PS paper) and evaporated in vacuo to yield N-benzyloxycarbonylpiperidin-4-ylethanol mesylate as a colourless paste (3.4 g) NMR (d6DMSO): δ0.9-1.2 (2H,m); 1.5-1.8 (5H,m);2.6-2.9 (2H,m); 4.0 (2H,d);4.25 (2H,t);4.4 (3H,s); 5.1 (2H,s); 7.35 (5H,m); m/e 342 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563141
Source datasetuspto-grants-1996_10
ORD IDord-0198cec58d5c4fff8ca81bff44b6db2e
Source noteuspto-grants-1996_10