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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1489447Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 54120013, compound

https://huagongshe.com/reaction/1489447

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 53712574HCID 53712574—
SolventDichloromethaneHCID 6344—
ProductHCID 54120013HCID 5412001383.2%

Reaction Steps

Under argon atmosphere, a solution of methyl (2S,3R)-2,3-dihydroxy-3-(4-fluorophenyl)propionate (3.95 g, 18.4 mmol) dissolved in dichloromethane (100 ml) was cooled to -3° to -5° C., and triethylamine (3.86 ml, 27.7 mmol) and p-toluenesulfonyl chloride (3.62 g, 19.0 mmol) were added to the solution. After the mixture was stirred at -3° to -5° C. for 44 hours, the reaction mixture was washed with water and brine. After the organic layer was dried over anhydrous sodium sulfate, the solvent was removed, and the residue obtained was purified by silica gel flash column chromatography (ethyl acetate/hexane=1/2) to obtain methyl (2S,3R)-3-(4-fluorophenyl)-3-hydroxy-2-p-toluenesulfonyloxypropionate (5.64 g, yield: 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05677470
Source datasetuspto-grants-1997_10
ORD IDord-bb2ba9d6de1140f99b45fa4231da1cc8
Source noteuspto-grants-1997_10