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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1415588Generated: November 1, 2026

1,2,4-Trichlorobenzene → HCID 69753798, compound

https://huagongshe.com/reaction/1415588

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2,4-TrichlorobenzeneHCID 13—
ReactantHCID 21483104HCID 21483104—
ReactantHCID 21483184HCID 21483184—
ProductHCID 69753798HCID 69753798—

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 3 parts of phenyl 3-chloro-2,6-dihydroxy-5-nitrobenzoate, 3 parts of 4-amino-α-(4-methoxyphenyl)-2-(trifluoromethyl)benzeneacetonitrile and 30 parts of 1,2,4-trichlorobenzene is stirred for 10 minutes at 190° C. The reaction mixture is cooled and poured onto 140 parts of petroleumether while stirring. The supernatant phase is decanted and the residue is boiled in methylbenzene and stirred with activated charcoal. The latter is filtered off over hyflo. Petroleumether is added to the filtrate till turbid and the product is allowed to crystallize while stirring. It is filtered off, dried and crystallized from acetonitrile, yielding 4.5 parts of 3-chloro-N-{4-[α-cyano-α-(4-methoxyphenyl)methyl]-3-trifluoromethyl)phenyl}-2,6-dihydroxy-5-nitrobenzamide; mp. 206.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04005218
Source datasetuspto-grants-1977_01
ORD IDord-5af04d60a18046a1a9318ce97d08beba
Source noteuspto-grants-1977_01