HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride, 4-chloro-3-nitro- → 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Methyloctadecylamine | HCID 75539 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 4-Chloro-N-methyl-3-nitro-N-octadecylbenzene-1-sulfonamide | HCID 19753711 | 71.2% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
In 300 ml of chloroform, 100 g of 4-chloro-3-nitrobenzenesulfonyl chloride was dissolved, and cooled to 0° C. Thereto, a solution of 84.3 g of methyloctadecylamine in chloroform was added dropwise. Then, 39.5 g of triethylamine was added dropwise as the reaction system was kept at a temperature from 0° C. to 10° C. After the conclusion of the addition, the reaction was run for 1 hour. Then, the solvent was distilled away, and the residue was dissolved in 500 ml of methanol under heating. The solution was allowed to stand for a while in order to cool. Thereupon, crystals separated out, and they were filtered off. Yield: 109 g, Percent yield: 71.2%, Melting point: 86°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05049477 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-92043e01933842cba172fbe0064fe547 |
| Source note | uspto-grants-1991_09 |