HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 2-Butyl-benzofuran-3-carbonyl chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2-Butyl-benzofuran-3-carboxylic acid | HCID 18505284 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Butyl-benzofuran-3-carbonyl chloride | HCID 18505346 | — |
Reaction Steps
Oxalyl Chloride (460 μL, 5.27 mmol) was added under nitrogen at room temperature to a solution of 2-butyl-benzofuran-3-carboxylic acid (230 mg, 1.05 mmol), prepared in the previous step, in 10 mL of methylene chloride. After the addition a catalytic amount of DMF was added and the reaction stirred at room temperature for 1.5 h. The solvent was removed under reduced pressure to give a brown oil. The oil was dissolved in benzene and the solvent removed under reduced pressure to give 2-butyl-benzofuran-3-carbonyl chloride as a brown oil. The material was immediately used in the following reaction with out additional purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07534894B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-042285b861754c4d87f5d248fbb90ee2 |
| Source note | uspto-grants-2009_05 |