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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268944Generated: October 30, 2026

Methanesulfonyl chloride → HCID 15550579, compound

https://huagongshe.com/reaction/2268944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2776577—
SolventDichloromethaneHCID 6344—
ProductHCID 15550579HCID 15550579—

Reaction Steps

To a stirred solution of 1-benzyloxycarbonyl-3-hydroxymethyl-piperidine (1.29 g, 5.24 mmol, 1 eq) in CH2Cl2 (50 mL) at 0° C. was added diisopropylethylamine (2.7 mL, 15.72 mmol, 3 eq) followed by methanesulfonylchloride (0.61 mL, 7.86 mmol, 1.5 eq) via syringe. Let stir 10 minutes and removed the cooling bath. After 30 minutes the reaction was complete by thin layer chromatography analysis. Removed the CH2Cl2 under reduced pressure and used material crude in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329380B1
Source datasetuspto-grants-2001_12
ORD IDord-8c19dd44dbd249858fc11d39bfd2cbd1
Source noteuspto-grants-2001_12