HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703475Generated: October 30, 2026
Benzenesulfonyl chloride, 3,4-dichloro- → 7-(n-Butyl)-3-[(3,4-dichlorophenyl)sulfonyl]-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane hydrochloride
https://huagongshe.com/reaction/703475
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride, 3,4-dichloro- | HCID 7383 | — |
| Reactant | 7-(n-Butyl)-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane | HCID 14369008 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-(n-Butyl)-3-[(3,4-dichlorophenyl)sulfonyl]-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane hydrochloride | HCID 22150350 | 127% |
Reaction Steps
A solution of 2.8 g (=0.0114 mol) 3,4-dichlorobenzene sulfonic acid chloride in 20 ml dichloromethane was added dropwise with ice cooling to a solution of 2.4 g (=0.0114 mol) 7-(n-butyl)-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane (=substance No. C1 in the following Table C) in 40 ml dichloromethane. Then the ice bath was removed and the reaction mixture stirred further for 3 hours at room temperature. The hydrochloride of the title compound thereby precipitated as a white precipitate. In order to complete crystallization, the reaction mixture was allowed to stand 12 more hours in a refrigerator. Then the crystals were separated by suction filtration and dried at 60° C. in a vacuum drier. 3.3 g 7-(n-butyl)-3-[(3,4-dichlorophenyl)sulfonyl]-9,9-dimethyl-3,7-diazabicyclo[3,3,1]nonane hydrochloride with a melting point of 170°-173° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04983611 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-872096aadfe244e4af44eefe02f735a5 |
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| Source note | uspto-grants-1991_01 |
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