HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 727735Generated: October 30, 2026
Benzenesulfonyl chloride, 4-chloro-3-nitro- → HCID 14324551, compound
https://huagongshe.com/reaction/727735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride, 4-chloro-3-nitro- | HCID 7323 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hexadecylamine | HCID 8926 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 14324551 | HCID 14324551 | — |
Reaction Steps
1 l of dichloromethane was added to 800 g of 4-chloro-3-nitrobenzenesulfonyl chloride. The admixture was cooled to a temperature of 0° C. A mixture of 600 g of hexadecylamine, 251 ml of triethylamine, and 780 ml of dichloromethane was added dropwise to the solution in such a manner that the temperature thereof was kept at 20° to 30° C. After being allowed to react at room temperature for 20 hours, dichloromethane was removed from the reaction mixture under reduced pressure. The residue was dissolved in 3 l of methanol under heating. The solution was gradually cooled to room temperature where crystallization took place. 3 of methanol was then added to the solution. The solution was cooled with ice to induce crystallization. The crystals were then
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USH0000963 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-647a5af5cc7c4508bb2bdf15c7623320 |
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| Source note | uspto-grants-1991_09 |
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