HuagongsheHuagongshe Chemistry Print Report · For research reference only
o-Phenetidine → 2-(2-Ethoxyanilino)methyl-4-propylmorpholine toluene-p-sulphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | o-Phenetidine | HCID 7203 | — |
| Reactant | 4-n-Propyl-2-toluene-p-sulphonyloxymethylmorpholine | HCID 21430362 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | 2-(2-Ethoxyanilino)methyl-4-propylmorpholine toluene-p-sulphonate | HCID 21519290 | — |
Reaction Steps
A solution of 2-ethoxyaniline (4.8 g.) and 4-n-propyl-2-toluene-p-sulphonyloxymethylmorpholine (10 g.) in xylene (50 ml.) is heated under reflux in an atmosphere of nitrogen for 60 hours. A resinous solid separates from the solvent which is distilled under reduced pressure. The residual sticky solid is washed with ether to give a yellow solid which is crystallised from methanol/ether to give 2-(2-ethoxyanilino)methyl-4-propylmorpholine toluene-p-sulphonate, m.p. 169°-172°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03974158 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-aba26f2c82b34e1e9d68b35ada05950b |
| Source note | uspto-grants-1976_08 |