Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 556303Generated: October 30, 2026

Triethylamine → 1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl ester

https://huagongshe.com/reaction/556303

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl piperidine-4-carboxylate hydrochlorideHCID 68664822—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-Methanesulfonyl-piperidine-4-carboxylic acid benzyl esterHCID 5742806378%

Reaction Steps

Piperidine-4-carboxylic acid benzyl ester, hydrochloride salt (1 g, 3.9 mmol, 1e.) from step 3, was dissolved in DMF (15 ml), Triethylamine (0.55 ml, 4 mmol, 1 eq.) and methanesulfonylchloride were added. The mixture was stirred for 1 h at room temperature, then was poured in water (20 ml). The aqueous solution was extracted with Ethyl Acetate (90 ml) and the organic layer was dried over anhydrous sodium sulfate, evaporated under reduced pressure to give a colourless oil. Yield 78%, 0.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058262B2
Source datasetuspto-grants-2011_11
ORD IDord-5dd2ee062b1c4a19b42dd555a4568765
Source noteuspto-grants-2011_11