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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090294Generated: October 31, 2026

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

https://huagongshe.com/reaction/2090294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—

Reaction Steps

To a solution of tert-butyl 4-hydroxypiperidine-1-carboxylate (5.03 g, 0.0250 mol, Aldrich Cat. No. 495484) in methylene chloride (50 mL) were added methanesulfonyl chloride (2.03 mL, 0.0262 mol, Aldrich, Cat. No. 471259) and triethylamine (3.66 mL, 0.0262 mol) at 0° C. The solution was stirred at r.t. overnight, then diluted with AcOEt, and washed with NaHCO3 aqueous solution and brine successively. The organic layer was dried with MgSO4 and then concentrated to afford the desired product which was directly used in next step. LCMS (M+Na)+: m/z=302.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436008B2
Source datasetuspto-grants-2013_05
ORD IDord-16495d8857b145c38525ec919a1468cb
Source noteuspto-grants-2013_05