HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112447Generated: October 27, 2026
4-Chlorobenzenesulfonyl chloride → HCID 131711316, compound
https://huagongshe.com/reaction/1112447
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | N-[[2-[3-(4-Morpholinyl)propoxy]phenyl]methyl]benzeneethanamine | HCID 21322756 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 131711316 | HCID 131711316 | — |
Reaction Steps
N-[[2-[3-(4-Morpholinyl)propoxy]phenyl]methyl]benzeneethanamine (14g, see Example 31C) is reacted with 9.2 g of p-chlorobenzenesulfonyl chloride in 130 ml of chloroform. A solution of the amine in chloroform is added dropwise at 10°-15° C to a stirred solution of the p-chlorobenzenesulfonyl chloride in chloroform. After the addition, the solution is stirred for 1 hour at room temperature and maintained for about 1 hour at room temperature. The chloroform is evaporated, and the residue is rubbed under ether. The resulting solid is taken up in acetonitrile, diluted with ether, rubbed and stored at a reduced temperature for several days, yielding 21.2 g of material, melting point 156°-158° C. Recrystallization from 130 ml of isopropanol yields 17 g of the title compound, melting point 163°-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04122255 |
|---|
| Source dataset | uspto-grants-1978_10 |
|---|
| ORD ID | ord-865b48b850614489bfd76fb5be350825 |
|---|
| Source note | uspto-grants-1978_10 |
|---|