HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-4-iodobenzene → 4-Acetyl-4'-chloro-2-nitrobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-4-iodobenzene | HCID 12510 | — |
| Reactant | 1-(4-Bromo-3-nitrophenyl)ethan-1-one | HCID 87737 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Acetyl-4'-chloro-2-nitrobiphenyl | HCID 21320563 | — |
Reaction Steps
4-Chloroiodobenzene and 4-bromo-3-nitroacetophenone were reacted under Ullmann conditions to give the novel intermediate 4-acetyl-4'-chloro-2-nitrobiphenyl, m.p. 103°-105° C. (from methanol). This compound was reduced with stannous chloride and concentrated hydrochloric acid to give 4-acetyl-2-amino-4'-chlorobiphenyl, m.p. 139°-140° C. (from methanol).This compound was converted to the novel intermediate 4-acetyl-4'-chloro-2-hydroxybiphenyl and thence to the novel intermediate 4-acetyl-4'-chloro-2-methoxybiphenyl, b.p. 167°-170° C./0.4 mm., by diazotization and methylation methods analogous to those described in Example 1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04048332 |
| Source dataset | uspto-grants-1977_09 |
| ORD ID | ord-36c8d562051a4322807182b29d42812f |
| Source note | uspto-grants-1977_09 |