HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 19838166, compound → HCID 22750172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 19838166 | HCID 19838166 | — |
| Reactant | 4-(2-Chloroethoxy)benzene-1-sulfonamide | HCID 22165154 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 22750172 | HCID 22750172 | 43.2% |
Reaction Steps
A mixture of N-2-(3,4-dibenzyloxyphenyl)ethyl benzylamine (13.6 g.), 2-(4-sulfamoylphenoxy)ethyl chloride (4.8 g.) and dry xylene (50 ml.) was boiled under reflux for 12 hours. The solution was cooled and the precipitated solid removed by filtration, the filtration then being evaporated in vacuo to dryness and taken up into diethyl ether. Insoluble material was removed from the ethereal solution by filtration, and the filtrate treated with ethereal hydrogen chloride, which resulted in the precipitation of a yellow solid. The latter was collected by filtration and recrystallized from a methanol/isopropanol mixture giving N-[2-(3,4-dibenzyloxyphenyl)ethyl]-N-[2-(4-sulfamoylphenoxy) ethyl] benzylamine hydrochloride (5.8 g.), m.p. 178°-181°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976783 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-51a0976d4db2460f999aa89f20b5e312 |
| Source note | uspto-grants-1976_08 |