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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463354Generated: October 31, 2026

Azobisisobutyronitrile → HCID 178468880, compound

https://huagongshe.com/reaction/463354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantChlorosuccinimideHCID 31398—
ReactantHCID 178468992HCID 178468992—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 178468880HCID 17846888087.2%

Reaction Conditions

Temperature65 °C

Reaction Steps

A mixture of 9.3 g of ethyl 2-ethyl-4-hydroxy-8-trifluoromethyl-3-quinoline-carboxylate, 200 ml of carbon tetrachloride, 4.2 g of N-chlorosuccinimide and 0.45 g of azobis-isobutyronitrile was stirred at 65° C. maximum for 5 hours under a lamp and was then cooled to 20° C. and was filtered. The filtrate was evaporated to dryness and the residue was taken up in methylene chloride. The mixture was washed with water, dried and evaporated to dryness. The residue was empasted with petroleum ether and dried to obtain 9 g of ethyl 2-(1-chloroethyl)-4-hydroxy-8-trifluoromethyl-3-quinoline-carboxylate melting at 104° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518775
Source datasetuspto-grants-1985_05
ORD IDord-6fb23fa673f444c8a362f40f19ffb14d
Source noteuspto-grants-1985_05