Hydrogen Peroxide → 5-(3-dimethylaminopropyl)-5-hydroxy-3-methylsulfonyl-5H-dibenzo[a,d]cycloheptene

HRID 2071737Notes

Reaction equation

HRID 2071737 reaction equation
[CH3:1][N:2]([CH3:24])[CH2:3][CH2:4][CH2:5][C:6]1([OH:23])[C:12]2[CH:13]=[C:14]([S:17][CH3:18])[CH:15]=[CH:16][C:11]=2[CH:10]=[CH:9][C:8]2[CH:19]=[CH:20][CH:21]=[CH:22][C:7]1=2.OO.S(=O)=[O:28].[OH-:30].[Na+]>C(O)(=O)C>[CH3:24][N:2]([CH3:1])[CH2:3][CH2:4][CH2:5][C:6]1([OH:23])[C:12]2[CH:13]=[C:14]([S:17]([CH3:18])(=[O:28])=[O:30])[CH:15]=[CH:16][C:11]=2[CH:10]=[CH:9][C:8]2[CH:19]=[CH:20][CH:21]=[CH:22][C:7]1=2

Participants

6

Procedure

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.

Workup

  1. addition, is added dropwise
  2. temperaturewith periodic cooling in an ice-bath
  3. extraction, and extracted with three 300 ml
  4. washAfter washing with combined extracts with water, solvent
  5. distillationis distilled under reduced pressure
  6. customleaving a yellow oily residue, weight 23.20 g
  7. customon standing at room temperature
  8. customFour recrystallizations from methanol-water
  9. customgives 13.22 g

Sources & evidence

ORD record
ord-fab73d8e979f438fa9271a1eb0463ff2
Source dataset
uspto-grants-1977_09
Patent number
US04048223

Reaction notes

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