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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1833485Generated: October 31, 2026

Water → 1-(p-Toluenesulfonyloxy)-4-acetoxy-5-(3-trifluoromethylphenoxy)pentane

https://huagongshe.com/reaction/1833485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant4-Acetoxy-5-(3-trifluoromethylphenoxy)-1-pentanolHCID 21317561—
SolventPyridineHCID 1049—
SolventDiethyl EtherHCID 3283—
Product1-(p-Toluenesulfonyloxy)-4-acetoxy-5-(3-trifluoromethylphenoxy)pentaneHCID 2131762994%

Reaction Steps

A solution of p-toluenesulfonyl chloride (65.2 g., 0.342 mole) in pyridine (130 ml.) is cooled in a cold water (10°-15°) bath while 4-acetoxy-5-(3-trifluoromethylphenoxy)-1-pentanol (90.7 g., 0.297 mole) is added dropwise with stirring during 70 minutes. The mixture is then stirred 2 hours in the same cold water bath. It is poured into 400 ml. of water. The oily product is taken up in ether, washed with water, 2N hydrochloric acid and dilute sodium bicarbonate solution and dried over magnesium sulfate. The solvent is evaporated in vacuo to leave 125 g. (94%) of the crude title compound as a nearly colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04066675
Source datasetuspto-grants-1978_01
ORD IDord-17e3abf0e17b444a9bc8c74d4ecc5b2c
Source noteuspto-grants-1978_01