HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2071737Generated: October 31, 2026
Hydrogen Peroxide → 5-(3-dimethylaminopropyl)-5-hydroxy-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene
https://huagongshe.com/reaction/2071737
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfur Dioxide | HCID 1119 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-(3-Dimethylaminopropyl)-5-hydroxy-3-methylmercapto-5H-dibenzo-[a,d]cycloheptene | HCID 53774404 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-(3-dimethylaminopropyl)-5-hydroxy-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene | HCID 21412087 | — |
Reaction Steps
5-(3-Dimethylaminopropyl)-5-hydroxy-3-methylmercapto-5H-dibenzo-[a,d]cycloheptene, 21.53 g. (0.063 mole), is dissolved in glacial acetic acid, 250 ml., and the solution is cooled in an ice-bath while 30% hydrogen peroxide, 25.8 ml., is added dropwise with stirring. After standing at room temperature for 22 hours, the solution is saturated with sulfur dioxide for 1 hour with periodic cooling in an ice-bath. The solution is made basic with 10 N. sodium hydroxide solution, 625 ml., and extracted with three 300 ml. portions of benzene. After washing with combined extracts with water, solvent is distilled under reduced pressure leaving a yellow oily residue, weight 23.20 g. The oil solidifies on standing at room temperature. Four recrystallizations from methanol-water gives 13.22 g. (57%) of product melting at 170°-171.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04048223 |
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| Source dataset | uspto-grants-1977_09 |
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| ORD ID | ord-fab73d8e979f438fa9271a1eb0463ff2 |
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| Source note | uspto-grants-1977_09 |
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