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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637864Generated: October 27, 2026

Formaldehyde → 1-(4-Chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-one

https://huagongshe.com/reaction/637864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
Reactantp-ChlorothiophenolHCID 7815—
ReactantPiperidineHCID 8082—
Reactant3,3-Dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanoneHCID 100877—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-(4-Chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-oneHCID 1319136528%

Reaction Steps

A mixture of 72.5 g (0.5 mol) of 4-chlorothiophenol, 100.2 g (0.6 mol) of 1,2,4-triazol-1-yl-pinacolin, 18 g (0.6 mol) of paraformaldehyde, 15 g of acetic acid and 5 ml of piperidine in 600 ml of toluene was heated under reflux in a water separator. After the water had been separated off, the reaction solution was washed with water, dried over sodium sulphate, filtered, and concentrated in vacuo. The oily residue was chromatographed over a silica gel column (mobile phase: chloroform). 45 g (28% of theory) of 1-(4-chlorophenylthio)-4,4-dimethyl-2-(1,2,4-triazol-1-yl)-pentan-3-one of melting point 67° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04559077
Source datasetuspto-grants-1985_12
ORD IDord-55fcba6076a7427b8be23bfa701bd6d6
Source noteuspto-grants-1985_12