HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-chloro-N-hexadecyl-N-methyl-3-nitrobenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 14324551 | HCID 14324551 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-chloro-N-hexadecyl-N-methyl-3-nitrobenzenesulfonamide | HCID 4162833 | 97% |
Reaction Steps
In 640 ml of acetone was dissolved 170 g of 4-chloro-3-nitro-N-hexadecylbenzenesulfonamide prepared in the above step and after adding thereto 79 g of potassium carbonate, 6 ml of polyethylene glycol (average molecular weight: 400), and 71 g of dimethylsulfuric acid, the mixture was refluxed for 5 hours. To the reaction mixture thus obtained was added 240 ml of acetone and after adding dropwise 870 ml or water to the mixture at 40° C., the resultant mixture was cooled to room temperature, whereby crystals deposited. The crystals were recovered by filtration, washed with water and then methanol, and dried to provide 169 g of the above-described compound with a yield of 97%. The melting point thereof was 74° C. to 75° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05071994 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-c27552ff90c946cea5fa512c213f9193 |
| Source note | uspto-grants-1991_12 |