HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | 1,3-Dibromodibenzo[b,d]furan-4-amine | HCID 58401066 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamide | HCID 58400857 | 70.3% |
Reaction Steps
In a 2 L round-bottomed flask, 1,3-dibromodibenzo[b,d]furan-4-amine (76 g, 223 mmol) in dichloromethane (800 mL) and pyridine (180 mL, 2229 mmol) were cooled by ice bath. Acetyl chloride (31.7 mL, 446 mmol) was added dropwise while stirring. Then the ice bath was removed. The reaction was stirred at room temperature for 1 h. The residue was collected by filtration and washed by water and dichloromethane to give N-(1,3-dibromodibenzo[b,d]furan-4-yl)acetamide (60 g, 70.3% yield) as brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156870B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-61240f818c4c40c08651ddf6cc23109d |
| Source note | uspto-grants-2015_10 |