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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374088Generated: November 1, 2026

Water → 4-(4-Cyanophenyl)butyl methanesulfonate

https://huagongshe.com/reaction/1374088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-(4-Hydroxybutyl)benzonitrileHCID 18540380—
SolventDichloromethaneHCID 6344—
Product4-(4-Cyanophenyl)butyl methanesulfonateHCID 18540424—

Reaction Steps

Methanesulfonyl chloride (2.32 mL, 30 mmol) was added to a cooled is (0° C.), stirred solution of 4-(4-hydroxybutyl)benzonitrile (from step (ii) above, 5.2 g, 29.7 mmol) and triethylamine (4.35 mL) in dichloromethane (50 mL). The resulting mixture was stirred for 4 h before water (150 mL) was added, and the organic layer separated, dried and concentrated to give the sub-title compound. This product was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07164017B2
Source datasetuspto-grants-2007_01
ORD IDord-edfef166958143b0bcc91c2e89d8d9cb
Source noteuspto-grants-2007_01