HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichlorobenzoyl chloride → (7-Ethyl-2-methyl-1H-indol-3-yl)(2,3-dichlorophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichlorobenzoyl chloride | HCID 17944 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 7-ethyl-2-methyl-1H-indole | HCID 22250587 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (7-Ethyl-2-methyl-1H-indol-3-yl)(2,3-dichlorophenyl)methanone | HCID 22250579 | 38.9% |
Reaction Steps
14.2 ml of 3M of MeMgI in Et2O are placed under argon and 6.78 g of 7-ethyl-2-methyl-1H-indole in 40 ml of Et2O are added dropwise. After 30 minutes, 17.84 g of 2,3-dichlorobenzoyl chloride in 60 ml of Et2O are added dropwise and the reaction medium is left stirring for 2 hours. The reaction medium is run quickly onto a saturated NH4Cl solution. The extraction is carried out with Et2O (twice) and then the organic phase is washed with a 10% NaOH solution, water and then a saturated NaCl solution. 5.5 g of the expected compound are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06995184B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-75d8e57cb69e4d6db7628b36c22d395f |
| Source note | uspto-grants-2006_02 |