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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723434Generated: November 3, 2026

Pyridine → (+)-(S)-3-(4-fluorophenoxy)-1,2-propanediol

https://huagongshe.com/reaction/1723434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant(-)-(R)-3-(4-fluorophenoxy)-1,2-propanediolHCID 11321370—
SolventChloroformHCID 6212—
Product(+)-(S)-3-(4-fluorophenoxy)-1,2-propanediolHCID 5364827467.2%

Reaction Steps

To a stirred mixture of 11 parts of (-)-(R)-3-(4-fluorophenoxy)-1,2-propanediol, 23.3 parts of pyridine and 240 parts of trichloromethane were added 12.3 parts of 4-methylbenzenesulfonyl chloride. The whole was stirred overnight at room temperature. It was washed successively with acid water, a sodium carbonate solution and water, dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (98:2 by volume) as eluent. The pure fractions were collected and the eluent was evaporated, yielding 13.5 parts (67.2%) of (+)-(S)-3-(4-fluorophenoxy)-1,2-propanediol, O1 -4-methylbenzenesulfonate; [α]D =+11.11° (c=0.5% in trichloromethane) (147).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04861785
Source datasetuspto-grants-1989_08
ORD IDord-e74a9cbc8aaa4a0686375f4c58b91253
Source noteuspto-grants-1989_08