HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → N-(2,3-Dihydro-1H-inden-2-yl)-N-propylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | N-propyl-2,3-dihydro-1H-inden-2-amine | HCID 17221237 | — |
| Product | N-(2,3-Dihydro-1H-inden-2-yl)-N-propylbenzamide | HCID 19041551 | 99% |
Reaction Steps
To a stirred solution of Indan-2-yl-propyl-amine (20.0 g, 114 mmol) in dichloro methane (200 mL) triethyl amine (17.4 mL, 125 mmol) was added. To this solution was then dropwise added benzoyl chloride (17.6 g, 125 mmol), followed by stirring at ambient temperature for 2 hours. The reaction was finally quenched by addition of dilute hydrochloric acid (50 mL, 10% HCl). The organic layer was separated, washed with water and dried over magnesium sulfate. Evaporation of the solvent yielded 31.5 g (99%) of the title compound as a dark oil.:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05639778 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-a7722a1462c24cf8994af2ec5e701262 |
| Source note | uspto-grants-1997_06 |