HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 3-Butyl-benzofuran-2-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Butyl-benzofuran-2-carboxylic acid | HCID 18505340 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Butyl-benzofuran-2-carbonyl chloride | HCID 18505360 | — |
Reaction Steps
Oxalyl Chloride (3.86 mL, 44.2 mmol) was added under nitrogen at room temperature to a solution of 3-butyl-benzofuran-2-carboxylic acid (1.93 g, 8.84 mmol) in 60 mL of methylene chloride. After the addition a catalytic amount of DMF (10 μL) was added and the reaction was stirred at room temperature for 2 h. The solvent was removed under reduced pressure. To remove the excess oxalyl chloride the residue was dissolved in benzene and the solvent removed under reduced pressure to give 3-butyl-benzofuran-2-carbonyl chloride, which was immediately used in step 2 without additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06589970B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-4620a0c77b894392b254633f88f49861 |
| Source note | uspto-grants-2003_07 |