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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284244Generated: October 31, 2026

Dimethylamine → 3-bromo-7-dimethylsulfamoyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-one

https://huagongshe.com/reaction/1284244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant3-bromo-7-fluorosulfonyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-oneHCID 21412111—
Solvent1,4-DioxaneHCID 31275—
Product3-bromo-7-dimethylsulfamoyl-10,11-dihydro-5H-dibenzo[a,d]-cyclohepten-5-oneHCID 21412094—

Reaction Steps

3-Bromo-7-fluorosulfonyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one (2.5 g., 0.00677 mole) together with 30 ml. of 25% aqueous dimethylamine and 30 ml. of p-dioxane is heated to refluxing for 3 hours. The brown solution is evaporated to dryness under reduced pressure and the residue partitioned between benzene and water. After washing with water, the benzene layer is evaporated to dryness under reduced pressure, leaving 3-bromo-7-dimethylsulfamoyl-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-5-one as a tan solid, m.p. 142°-145°C., in a yield of 2.1 g. (80%). An analytical sample melts at 146°-148°C. after crystallizations from mixtures of benzene and hexane and from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03978121
Source datasetuspto-grants-1976_08
ORD IDord-b8089c8ab01c464896d0914aa75b2f3a
Source noteuspto-grants-1976_08