HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 58368355, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4-(2-Fluoro-4-nitrophenoxy)pyrrolo[1,2-b]pyridazine | HCID 58799006 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 58368355 | HCID 58368355 | 93% |
Reaction Steps
AlCl3 (1.46 g, 10.98 mmol) was added to a solution of 4-(2-fluoro-4-nitrophenoxy)pyrrolo[1,2-b]pyridazine (600 mg, 2.19 mmol) in dichloroethane (60 mL). After stirring at room temperature for 1 hour and adding acetyl chloride (0.17 mL, 2.42 mmol), the mixture was further stirred for 3 hours. The resulting reaction mixture was neutralized with saturated sodium bicarbonate aqueous solution. The resulting mixture was filtered through celite. After phase separation of the filtrate, the organic layer was dried with magnesium sulfate and then filtered. The filtrate was concentrated and then purified by silica gel chromatography (1-6% ethyl acetate in dichloromethane) to give the target compound as a white solid (640 mg, 2.03 mmol, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957102B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-29d0495e48954bd9b9a381956d7e888a |
| Source note | uspto-grants-2015_02 |