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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2,4-Trichlorobenzene | HCID 13 | — |
| Reactant | HCID 21483104 | HCID 21483104 | — |
| Reactant | HCID 21483184 | HCID 21483184 | — |
| Product | HCID 69753798 | HCID 69753798 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04005218 |
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| Source dataset | uspto-grants-1977_01 |
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| ORD ID | ord-5af04d60a18046a1a9318ce97d08beba |
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| Source note | uspto-grants-1977_01 |
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