HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → 2-benzoyl-N-[2-(p-toluenesulfonamido)ethyl]-N-isopropylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | 2-Benzoylbenzoic Acid | HCID 6813 | — |
| Reactant | N-[2-(isopropylamino)ethyl]-p-toluenesulfonamide | HCID 21568614 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-benzoyl-N-[2-(p-toluenesulfonamido)ethyl]-N-isopropylbenzamide | HCID 53759036 | — |
Reaction Steps
A solution of 37 grams of ψ-acid chloride of 0-benzoyl benzoic acid in 60 ml. of dichloromethane was added dropwise to a stirred solution of 38.5 grams of N-[2-(isopropylamino) ethyl]-p-toluenesulfonamide, 200 ml. of dichloromethane and 25 ml. of triethylamine. The mixture was refluxed for 3.5 hours. After cooling, the solution was extracted successively with water, 10% hydrochloric acid, and saturated sodium carbonate solution. The dichloromethane solution was dried over magnesium sulfate and the solvent evaporated in vacuo to a solid residue. On recrystallization from ethyl acetate there was obtained 2-benzoyl-N-[2-(p-toluenesulfonamido)ethyl]-N-isopropylbenzamide, m.p. 135°-137°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03931218 |
| Source dataset | uspto-grants-1976_01 |
| ORD ID | ord-13f7c8a9f74244558866f4ef2dc7d38a |
| Source note | uspto-grants-1976_01 |