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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383367Generated: October 26, 2026

Methanesulfonyl chloride → HCID 22600111, compound

https://huagongshe.com/reaction/1383367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl N-(4-chloro-3-(hydroxymethyl)phenyl)carbamateHCID 54223790—
SolventDichloromethaneHCID 6344—
ProductHCID 22600111HCID 22600111100%

Reaction Steps

To an ice cooled solution of 2-chloro-5-(Boc-amino)benzyl alcohol (7.4 g; 29 mmol; from step (i) above) in CH2Cl2 (100 mL) was added TEA (2.9 g; 29 mmol), followed by MsCl (3.3 g, 29 mmol; added dropwise). After stirring for 2 hours the resultant mixture was poured onto water. The organic layer was separated, washed with water, dried (Na2SO4) and concentrated to yield 10 g (100%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255301B1
Source datasetuspto-grants-2001_07
ORD IDord-3f310dfb18e84bfd841c2b975d707a6b
Source noteuspto-grants-2001_07