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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434527Generated: October 31, 2026

Azobisisobutyronitrile → HCID 178468880, compound

https://huagongshe.com/reaction/434527

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 numberUS04397856
Source datasetuspto-grants-1983_08
ORD IDord-dfbda01657ad406cb13bf6cc87964d7c
Source noteuspto-grants-1983_08