HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Reactant | N-Methyloctadecylamine | HCID 75539 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide | HCID 19753711 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
300 ml of chloroform was added to 100 g of 4-chloro-3-nitrobenzenesulfonyl chloride. The solution was then cooled to a temperature of 0° C. A chloroform solution of 84.3 g of methyloctadecylamine was added dropwise to the solution. 39.5 g of triethylamine was then added dropwise to the solution while the temperature thereof was kept at 0° to 10° C. The solution was stirred at room temperature for 1 hour. Chloroform was removed from the solution under reduced pressure. 500 ml of methanol was added to the residue. The reaction mixture was heated to complete dissolution. The solution was cooled., The resulting crystals were filtered off and dried. (Yield: 109 g (71%); m.p.: 86°-87° C.)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USH0000963 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-6e993effdf964c4fad692a00f31a6c69 |
| Source note | uspto-grants-1991_09 |