HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868303Generated: October 31, 2026
Hydrochloric Acid → HCID 15052915, compound
https://huagongshe.com/reaction/868303
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,4,5-Trichloronitrobenzene | HCID 88365 | — |
| Reactant | 4-Chlorobenzyl cyanide | HCID 241582 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15052915 | HCID 15052915 | 93.3% |
Reaction Steps
To a stirred mixture of 45.3 parts of 1,2,3-trichloro-5-nitrobenzene, 300 parts of a sodium hydroxide solution 50%, 5 parts of N,N,N-triethylbenzenemethanaminium chloride and 360 parts of tetrahydrofuran was added dropwise, during a 5 minute period, a solution of 33.3 parts of 4-chlorobenzeneacetonitrile in 90 parts of tetrahydrofuran. Upon completion, stirring was continued for 4 hours at 50° C. The reaction mixture was poured into 1500 parts of crushed ice and acidified with concentrate hydrochloric acid. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was stirred in 2,2'-oxybispropane. The product was filtered off and dried, yielding 63.8 parts (93.3%) of 2,6-dichloro-α-(4-chlorophenyl)-4-nitrobenzeneacetonitrile (intermediate 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04778887 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-117d25d03b7e4a3787c11890557f93bc |
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| Source note | uspto-grants-1988_10 |
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