HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → (4-Chloro-phenyl)-(4,5-difluoro-2-iodo-phenyl)-diazene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-Chloro-4-nitrosobenzene | HCID 13614 | — |
| Reactant | 4,5-Difluoro-2-iodoaniline | HCID 12181913 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | (4-Chloro-phenyl)-(4,5-difluoro-2-iodo-phenyl)-diazene | HCID 86640263 | 27% |
Reaction Steps
Chloro-4-nitroso-benzene (9.1 g, 64 mmol; [932-98-9]) was added to a solution of 4,5-difluoro-2-iodo-phenylamine (10.9 g, 43 mmol; [847685-01-2]) in acetic acid (430 ml). The reaction mixture was heated under reflux conditions for 14 h. Ice water (1 l) and EtOAc (1 l) was added, the layers were separated and the aqueous layer was extracted two times with EtOAc. The combined extracts were washed with water and brine and dried over Na2SO4. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica gel, CH2Cl2/heptane) to give the title compound (4.34 g, 11 mmol; 27%) as orange solid. MS: m/e=377.9 [M+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153663B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-573ef9d7b8a340d18c5bc0e62fae1cba |
| Source note | uspto-grants-2012_04 |