HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Methoxyphenyl 4-methoxy-1-naphthyl sulfone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,2-Dichlorobenzene | HCID 7239 | — |
| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | 1-Methoxynaphthalene | HCID 16668 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | 4-Methoxyphenyl 4-methoxy-1-naphthyl sulfone | HCID 16226212 | 88% |
Reaction Steps
p-Methoxybenzenesulfonyl chloride, 2.0 mol, anhydrous stannic chloride, 2.25 mol, 1-methoxynaphthalene, 2.25 mol, and 3 1 of o-dichlorobenzene were mixed at room temperature under nitrogen. The mixture was stirred at room temperature overnight (ca 7 hours needed) and decomposed with 3N hydrochloric acid. The organic layer was diluted with 1250 ml of nitromethane and washed with 2 portions of 1N hydrochloric acid followed by pure water. The organic layer was treated with magnesium sulfate, filtered, evaporated, extracted with hot toluene and dried at 120° C. for two hours to give 577 g, 88% yield, m.p. 160°-162° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04996279 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-7b9de6f2523346099b89ad86ffdc73bb |
| Source note | uspto-grants-1991_02 |