HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 20290850, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 451690 | HCID 451690 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 20290850 | HCID 20290850 | — |
Reaction Steps
To a solution of 4,5-bis(4-methoxyphenyl)-2-nitroimidazole (3.0 g, 9.22 mmole) and triethylamine (7 ml., 51 mmole) in 30 ml. THF at 0° C. under N2 was dropwise added a solution of acetyl chloride (1.3 ml., 18.4 mmole) in 5 ml. THF. After 2 hours at 0° C., the reaction mixture was diluted with ethyl acetate washed with 1N HCl, saturated aqueous NaHCO3 and brine, dried and concentrated on a rotary evaporator. Crystallization from ether gave approximately 600 mg. of starting material. HPLC of the mother liquor and crystallization from ether gave 1-acetyl 4,5-bis(4-methoxyphenyl)-2-nitroimidazole, mp. 146°-151° C. H-NMR indicates purity >95%. H-NMR: 2.41δ (s, 3H), 3.8δ (s, 3H), 6.73-7.56 δ(2AB quartets, J=9Hz, 8H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04251535 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-8f9124bce5bf4f5b978bdfc8e9351428 |
| Source note | uspto-grants-1981_02 |