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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 51249Generated: October 25, 2026

Dichloromethane → 4-Fluorophenethyl alcohol methanesulfonate

https://huagongshe.com/reaction/51249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Fluorophenethyl AlcoholHCID 82068—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
Product4-Fluorophenethyl alcohol methanesulfonateHCID 15036433102.7%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

A suitable reactor maintained under nitrogen was charged with 4-fluorophenethyl alcohol (2.6 kg, 18.6 mol) and 18 L of methylene chloride. The stirred solution was cooled to and maintained at 0-5° C. while triethylamine 2.85 kg (28.2 mol) was added fairly rapidly. The reaction temperature was maintained at 0-5° C. while adding methanesulfonyl chloride (2.5 kg, 21.8 mol) over 1 hour. The stirred reaction mixture was maintained at 0-5° C. for 1 hour, then it was warmed to room temperature within approximately 2 hours. The reaction mixture was diluted with a solution of 0.5 kg of 33% hydrochloric acid in 10 L of water. The organic phase was separated and washed with a solution of 0.2 kg of 33% hydrochloric acid in 5 L of water. Both acidic extracts were combined and extracted with 5 L of methylene chloride. Both organic phases were combined, washed with 2×15 L of water, then dried with sodium sulfate (2 kg). Drying agent was filtered off and washed with 2×5 L of methylene chloride. The majority of the solvent was boiled off at atmospheric pressure, with the final amount distilled off at 35° C./500 torr to give 4-fluorophenethyl alcohol methanesulfonate (4.17 kg.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06713627B2
Source datasetuspto-grants-2004_03
ORD IDord-f2ed1e239bf64572844dd9fd847cfe67
Source noteuspto-grants-2004_03