HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Methyl-4-aminobiphenyl hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Methyl-4-acetaminobiphenyl | HCID 11172156 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Methyl-4-aminobiphenyl hydrochloride | HCID 18533491 | — |
Reaction Steps
300 g of water and 296 g of HCl (37%) are added to the 2-methyl-4-acetaminobiphenyl prepared as described in Example 1. Any chlorobenzene still present is distilled off azeotropically, and the mixture is subsequently refluxed until HPLC monitoring indicates complete conversion (about 4 hours). The suspension obtained can be reacted further without further purification and without removal of the acetic acid formed as coproduct in the cleavage. The yield is (calculated from HPLC percentages by area) 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06566546B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-8a894b2f7d324691a6aeecead6b50a5b |
| Source note | uspto-grants-2003_05 |