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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2245391Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 67410578, compound

https://huagongshe.com/reaction/2245391

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 11815996HCID 11815996—
Reactant1-phenyltetrazole-5-thiolHCID 178527986—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductHCID 67410578HCID 6741057899.9%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of (1S)-1-(1-ethylcyclobutyl)-propane-1,3-diol (8.90 g) in toluene (110 mL) were added tetrabutylammonium chloride (1.56 g) and a 2N aqueous sodium hydroxide solution (170 mL). At an inner temperature about 25° C., tosyl chloride (11.3 g) was added to the reaction solution, which was stirred at 25° C. for 1 hour. 1-Phenyl-1H-tetrazol-5-thiol (11.0 g) was added to the reaction solution, which was stirred at 60° C. for 1 hour. After cooling, water was added to the reaction solution, which was separated. The water layer was extracted with t-butyl methyl ether. The mixed organic layer was washed with water and brine, dried over anhydrous magnesium sulfate and concentrated to give the title compound (17.9 g) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07683094B2
Source datasetuspto-grants-2010_03
ORD IDord-d0154685fabc4fc793a150c676448d10
Source noteuspto-grants-2010_03