HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 1-benzylindole-3-carbonyl Chloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 1-benzyl-1H-indole-3-carboxylic acid | HCID 33671 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-benzylindole-3-carbonyl Chloride | HCID 10492228 | 100% |
Reaction Steps
A mixture of 1-benzyl-1H-indole-3-carboxylic acid (3.36 g, 13.37 mmol), oxalyl chloride (5.83 mL, 66.85 mmol), 100 mL methylene chloride and a catalytic amount of DMF was stirred at room temperature under nitrogen for 18 h (overnight). The solvent was removed under reduced pressure. To remove excess oxalyl chloride benzene was added and the solvent removed under reduced pressure to give 1-benzyl-1H-indole-3-carbonyl chloride as a brown oil (13.37 mmol) 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-0bf60df8a1c74795bc21d394634198d6 |
| Source note | uspto-grants-2003_07 |