HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanobenzoic acid → 2-Cyanobenzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanobenzoic acid | HCID 12087 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Phosphorus trichloride | HCID 24387 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Hydroxyethyl 7-[[4-(morpholinoiminomethyl)benzoyl]amino]-1,2,3,4-tetrahydronaphthalene-2-acetate | HCID 70075691 | — |
| Reactant | 2-Methoxyethyl 7-[[4-(morpholinoiminomethyl)benzoyl]amino]-1,2,3,4-tetrahydronaphthalene-2-acetate | HCID 70076126 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Cyanobenzoyl chloride | HCID 119681 | — |
Reaction Steps
In another process, p-cyanobenzoic acid or the compounds of formula (4) or (5) is reacted with thionyl chloride, oxalyl chloride, phosphorus trichloride, phosphorus pentachloride or phosphorus oxychloride in the presence of a catalytic amount of N,N-dimethylformamide to give o-cyanobenzoyl chloride or the compounds of formula (6) or (7). p-Cyanobenzoyl chloride or the compounds of formula (6) or (7) thus obtained can be reacted with the compounds of formula (2) or (3), or the compounds of formula (8) to give the desired compounds.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05719145 |
| Source dataset | uspto-grants-1998_02 |
| ORD ID | ord-2632740d011b4b11a0deb2b93ca10774 |
| Source note | uspto-grants-1998_02 |