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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1153965Generated: October 30, 2026

4-Toluenesulfonyl chloride → HCID 86739786, compound

https://huagongshe.com/reaction/1153965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactantp-ToluenesulfonateHCID 85570—
ReactantHCID 10379527HCID 10379527—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86739786HCID 86739786—

Reaction Steps

The alcohol is converted to the tosylate by dissolving in methylene chloride containing N,N-dimethyl-4-aminopyridine (0.05 mol eq) and triethylamine (1.05 mol eq) and treating with tosyl chloride (1.1 mole eq) added in one portion at 0° C. with stirring. After standing for about 24 hr. at 0° C., the mixture is treated with water and extracted several times with methylene chloride. The combined methylene chloride extracts are dried over magnesium sulfate, filtered and concentrated under reduced pressure. Flash chromatography of residual material affords 2-[3-(p-toluenesulfonate)propyl]-5-ethyl-2,4-dihydro-4-(2-phenoxyethyl)-3H-1,2,4-triazol-3-one (XV, Y=H, X1 =0, n=2, R2 =C2H5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04487773
Source datasetuspto-grants-1984_12
ORD IDord-ca12cd3df928430db815c350cc4a9720
Source noteuspto-grants-1984_12