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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 14502060HCID 14502060—
SolventMethanolHCID 887—
ProductHCID 14502061HCID 1450206153.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04849441
Source datasetuspto-grants-1989_07
ORD IDord-fba7940cd16b4887ba9d875ed6bb9aa2
Source noteuspto-grants-1989_07