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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388997Generated: November 2, 2026

Chloroacetyl chloride → HCID 20213180, compound

https://huagongshe.com/reaction/1388997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
ReactantHCID 20213179HCID 20213179—
SolventTolueneHCID 1140—
ProductHCID 20213180HCID 2021318098.2%

Reaction Steps

To a stirred solution of 6.1 g (0.0232 mol) 3-(2,6-dimethylphenylamino)-4-methyl-5-methylthio-1,2,4-triazole in 150 ml toluene was added quickly 2.7 g (0.024 mol) chloroacetyl chloride. An exotherm ensued and the temperature rose to 100° C., followed by separation of an oil which solidified. The reaction mixture was stirred at 100°-105° C. for 1 hour, cooled and diluted with 50 ml saturated sodium bicarbonate and 20 ml dichloromethane. The clear organic layer was separated, dried over magnesium sulfate and evaporated under reduced pressure to give a clear oil. The oil was crystallized from ethyl ether to give 7.4 g of product, as a pale yellow solid, m.p. 145°-147° C. The product is tabulated in Table I as Compound No. 14-B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243408
Source datasetuspto-grants-1981_01
ORD IDord-e5497dffc1aa439fa6229978dbce9c63
Source noteuspto-grants-1981_01