Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712057Generated: October 30, 2026

Methanesulfonyl chloride → HCID 86717515, compound

https://huagongshe.com/reaction/712057

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86717516HCID 86717516—
SolventDichloromethaneHCID 6344—
ProductHCID 86717515HCID 8671751592%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of tert-butyl [(1S,3S,4R)-4-(hydroxymethyl)-3-methoxycyclohexyl]carbamate (racemic) (720 mg, 2.8 mmol) in dichloromethane (9 mL) was added methanesulfonyl chloride (0.430 mL, 5.56 mmol) at 0° C. The mixture was stirred at 0° C. for 1 h. The mixture was then concentrated and partitioned between ethyl acetate and water. The organic phase was concentrated and purified by flash chromatography (eluting with a gradient of 50% ethyl acetate in hexanes) to give the desired product (0.859 g, 92%). LCMS calculated for C9H20NO4S (M+H-Boc)+: m/z=238.1. Found: 238.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181271B2
Source datasetuspto-grants-2015_11
ORD IDord-fad0a06d13ce469abf562f2526f0100c
Source noteuspto-grants-2015_11