HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231867Generated: October 30, 2026
p-Toluenesulfonic acid monohydrate → HCID 14502061, compound
https://huagongshe.com/reaction/231867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 14502060 | HCID 14502060 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 14502061 | HCID 14502061 | 53.4% |
Reaction Steps
In 300 ml of methyl alcohol was dissolved 22.45 g of 3-(2-amino-3, 5-dimethylphenyl)-1, 3-dihydroisobenzofuran-1-one. The solution was heated at reflux for 10 hours in the presence of 20.23 g of p-toluenesulfonic acid monohydrate. The resulting solution was concentrated to dryness under reduced pressure. The obtained solid was dissolved in 200 ml of dichloromethane. The solution was washed with saturated aqueous sodium bicarbonate solution and with saturated aqueous sodium chloride solution. After drying over anhydrous sodium sulfate, the solution was filtered and the resulting filtrate was concentrated to dryness under reduced pressure. To the obtained solid was added to diisopropyl ether and the solid was ground into powders. Thus, 12.65 g of 2,4-dimethyl-11-methoxy-5, 11-dihydro-6H-dibenz[b,e]azepin-6-one was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04849441 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-fba7940cd16b4887ba9d875ed6bb9aa2 |
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| Source note | uspto-grants-1989_07 |
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