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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249369Generated: November 2, 2026

Thioglycolic Acid → HCID 13770337, compound

https://huagongshe.com/reaction/1249369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioglycolic AcidHCID 1133—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 13770336HCID 13770336—
SolventWaterHCID 962—
ProductHCID 13770337HCID 1377033750%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 11.1 parts of 2-[3-chloro-4-[1-(4-chlorophenyl)-1-cyanoethyl]-5-methylphenyl]-2,3,4,5-tetrahydro-3,5-dioxo-1,2,4-triazine-6-carboxylic acid and 15 parts of 2-mercaptoacetic acid was stirred and heated for 2 hours at 180° C. The reaction mixture was cooled, water was added and the whole was treated with sodium hydrogen carbonate. The product was extracted with trichloromethane. The organic layer was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (95:5 by volume) as eluent. The pure fractions were collected and the eluent was evaporated in vacuo. The residue was stirred in 2,2'-oxybispropane. The product was filtered off and dried, yielding 5 parts (50%) of 2-chloro-α-(4-chlorophenyl)-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-α,6-dimethylbenzeneacetonitrile; mp. 226.7° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04631278
Source datasetuspto-grants-1986_12
ORD IDord-997c31912f7845598b34f6fe2cd6c707
Source noteuspto-grants-1986_12