HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 59424944, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 59425917 | HCID 59425917 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59424944 | HCID 59424944 | 100.9% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A suspension of 3-cyano-1-ethyl-1H-indole-6-carboxylic acid (0.42 g, 1.96 mmol) in CH2Cl2 (15 mL) is cooled to 0° C. The suspension is treated with DMF (2 drops) and then oxalyl chloride (0.34 mL, 3.92 mmol) is added via syringe during 2 minutes after which the ice bath is removed and the reaction mixture is allowed to warm to ambient temperature during 1.5 h during which time the reaction becomes a yellow solution. The solution is then concentrated in vacuo to afford 0.46 g (quantitative yield) of 3-cyano-1-ethyl-1H-indole-6-carbonyl chloride as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07781478B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-2115d6df555b4ed4b8f11209b1a3d87f |
| Source note | uspto-grants-2010_08 |