Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397658Generated: October 25, 2026

Triethylamine → HCID 57106621, compound

https://huagongshe.com/reaction/397658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexylmethane sulfonyl chlorideHCID 3871475—
Reactantmethyl (2S)-piperidine-2-carboxylate hydrochlorideHCID 13246232—
SolventDichloromethaneHCID 6344—
ProductHCID 57106621HCID 5710662170.5%

Reaction Steps

Triethylamine (22.15 ml) was added to a solution of (2S)-2-(methoxycarbonyl)piperidine hydrochloride (10 g) [see Preparation 24] and cyclohexylmethanesulfonyl chloride (16.42 g) [King. J. F. et al,. J. Am. Chem. Soc., 1992, 114(5), 1743-9] in dichloromethane (100 ml). The reaction mixture was stirred for 18 hours after which time the solvent was removed under reduced pressure and the residue diluted with ethyl acetate. The organic layer was washed with water, brine, dried over magnesium sulphate and the solvent was removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 95:5 changing to 80:20, by volume, hexane:ethyl acetate to afford methyl (2S)-1-[(cyclohexylmethyl)sulfonyl]-2-piperidinecarboxylate (11.9 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-8fae7256d29a449793106bcdde891b9f
Source noteuspto-grants-2003_08