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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869205Generated: October 30, 2026

Methanesulfonyl chloride → Methanesulfonic acid 3-chloro-1-phenyl-propyl ester

https://huagongshe.com/reaction/1869205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-Chloro-1-phenylpropanolHCID 572064—
SolventDichloromethaneHCID 6344—
ProductMethanesulfonic acid 3-chloro-1-phenyl-propyl esterHCID 57985877—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the 3-chloro-1-phenyl-propan-1-ol (1.5 g, 8.79 mmol) in DCM at 0° C. (50 mL) was added TEA (1.6 mL, 11.4 mmol) followed by MsCl (0.75 mL, 9.7 mmol). The reaction mixture was stirred 1.5 hours at 0° C., quenched with ice, and partitioned between a saturated solution of NaHCO3 and DCM. The organic layer was separated, washed with brine, dried over MgSO4, filtered, and concentrated at 0° C. The methanesulfonic acid 3-chloro-1-phenyl-propyl ester (95% crude yield, 2.08 g) thus prepared was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638517B2
Source datasetuspto-grants-2009_12
ORD IDord-1b8b2c5dbf29486ba74bc3a644092bb7
Source noteuspto-grants-2009_12