Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexadecylamine | HCID 8926 | — |
| Reactant | 2-chloro-3-nitrobenzene-1-sulfonyl chloride | HCID 23042488 | — |
| Product | HCID 14324551 | HCID 14324551 | — |
Reaction Steps
1 liter of dichloromethane was added to 800 g of 4 chloro-3-nitrobenzenesulfonyl chloride and cooled to 0° C. To the solution was added dropwise a mixture comprising 600 g of hexadecylamine, 251 ml of triethylamine and 780 ml of dichloromethane at 20 to 30° C. After being reacted for 2 hours at room temperature, the dichloromethane was removed by distillation under reduced pressure, and 3 liters of methanol was added to the residue and dissolved under heat. The resulting solution was gradually cooled and crystallized out at room temperature. Further, 3 liters of methanol was added and the resulting solution was again crystallized out under ice-cooling, and the crystal precipitated was taken out by filtration and dried. Yield: 1020 g, 88%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04942114 |
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| Source dataset | uspto-grants-1990_07 |
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| ORD ID | ord-ee1e3749116e462ea44fbd8321ffe9d5 |
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| Source note | uspto-grants-1990_07 |
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