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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084739Generated: October 29, 2026

Dichloromethane → 4-(2-Fluorophenyl)-3-hydroxy-2-methylbutyl tosylate

https://huagongshe.com/reaction/2084739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant4-(2-Fluorophenyl)-3-hydroxy-2-methylbutane-1,3-diolHCID 22734650—
SolventWaterHCID 962—
Product4-(2-Fluorophenyl)-3-hydroxy-2-methylbutyl tosylateHCID 1207057488%

Reaction Steps

Under a nitrogen atmosphere, a mixture of 13.5 g (68.1 mmol) of 4-(2-fluorophenyl)-3-hydroxy-2-methylbutane-1,3-diol, 14.2 ml (21.3 mmol) of triethylamine, and 70 ml of dichloromethane was cooled with an ice bath and 13.0 g (68.1 mmol) of p-toluenesufonyl chloride was added to the mixture. After stirring overnight at room temperature, 100 ml of water was added thereto, followed by extraction 3 times each with 200 ml of dichloromethane, and the combined organic layer was dried with anhydrous sodium sulfate. After drying, the solvent was distilled off and the residue was purified by silica gel column chromatography to obtain 21.1 g of the title compound as a colorless oil. (Yield: 88%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06717016B2
Source datasetuspto-grants-2004_04
ORD IDord-4e56efa2cda5482fb900e092ba09a00d
Source noteuspto-grants-2004_04