HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → Benzoyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 7-(4-Aminoanilino)-4-hydroxynaphthalene-2-sulfonic acid | HCID 117154 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzoyl chloride | HCID 7412 | — |
| Product | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Product | Benzoyl chloride, 3-chloro- | HCID 69252 | — |
Reaction Steps
16.5 parts of 6-(4'-aminophenylamino)-1-hydroxynaphthalene-3-sulfonic acid are dissolved in 1500 parts of hot water. After cooling down to room temperature, 9.65 parts of 4-chlorobenzoyl chloride are added dropwise in the course of about 30 minutes and the reaction mixture is reacted at a pH maintained at 6 until the consumption of sodium hydroxide solution has ceased (duration about 2.5 to 4 hours). Then the pH is adjusted to 1 with hydrochloric acid and the product is salted out with sodium chloride. Filtering off with suction and drying gives the compound of the formula ##STR72## The replacement of 4-chlorobenzoyl chloride with an equivalent amount of benzoyl chloride or 3-chlorobenzoyl chloride gives analogous intermediates.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05225545 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-b0a1af2c6420433f8e798ea5ba82c7f8 |
| Source note | uspto-grants-1993_07 |