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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079657Generated: October 30, 2026

Triethylamine → 1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidine

https://huagongshe.com/reaction/2079657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—

Reaction Steps

To tert-butyl 4-hydroxypiperidine-1-carboxylate (1 eq) in methylene chloride and triethyl amine (1.4 eq) at 0° C. was added methane sulfonyl chloride (1.4 eq) drop-wise. The reaction was brought to ambient temperature and was stirred for 1 h. The reaction mixture was washed with water and saturated sodium chloride solution. The organic layer was then dried with sodium sulfate and concentrated to yield tert-butyl-4-(methylsulfonyloxy)piperidine-1-carboxylate in quantitative yield. The product was confirmed by 1H NMR, and used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932262B2
Source datasetuspto-grants-2011_04
ORD IDord-0261cb0981124ee48b37da971e2a25f0
Source noteuspto-grants-2011_04