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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290546Generated: October 30, 2026

Triethylamine → HCID 86638743, compound

https://huagongshe.com/reaction/1290546

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 (3×) 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) δ 0.9-1.2(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 numberUS05750754
Source datasetuspto-grants-1998_05
ORD IDord-e469c09be9db4cbf813507f451af1a07
Source noteuspto-grants-1998_05