1,2-Dichloroethane → HCID 69851286, compound

HRID 1740891Notes

Reaction equation

HRID 1740891 reaction equation
I(Cl)(=O)=O.I(Cl)(=O)=[O:6].C([N+](C)(C)C)[C:10]1[CH:15]=CC=CC=1.C(C1[CH:33]=[C:32]([C:34]([CH3:37])([CH3:36])[CH3:35])[C:26]2[O:27][CH2:28][C:29]([CH3:31])([CH3:30])[C:25]=2C=1)(=O)C.Cl[CH2:39][CH2:40][Cl:41]>CO>[Cl:41][C:40]1[CH:33]=[C:32]([C:34]([CH3:35])([CH3:36])[CH3:37])[C:26]2[O:27][CH:28]([C:15](=[O:6])[CH3:10])[C:29]([CH3:30])([CH3:31])[C:25]=2[CH:39]=1

Participants

5

Procedure

A mixture of benzyltrimethylammonium dichloroiodate (31:70 g, 91.0 mmol), 5-acetyl-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan (12.35 g, 50.2 mmol), 300 mL of 1,2-dichloroethane, and 120 mL of methanol is heated at reflux for 13 h. The reaction mixture is cooled to room temperature and concentrated in vacuo; 5% aqueous sodium bisulfite solution (125 mL) is added to the residue obtained. This mixture is extracted with ether; the extract is washed with aqueous sodium bicarbonate solution and with brine, dried over anhydrous magnesium sulfate, and concentrated to produce about 14.09 g (100%) of 5-chloro-acetyl-7-tert-butyl-2,3-dihydro-3,3-dimethylbenzo[b]furan as a reddish solid: mp 76-77° C.

Workup

  1. temperatureis heated
  2. temperatureat reflux for 13 h
  3. concentrationconcentrated in vacuo
  4. addition5% aqueous sodium bisulfite solution (125 mL) is added to the residue
  5. customobtained
  6. extractionThis mixture is extracted with ether
  7. washthe extract is washed with aqueous sodium bicarbonate solution and with brine
  8. dry with materialdried over anhydrous magnesium sulfate
  9. concentrationconcentrated

Sources & evidence

ORD record
ord-14280f820e3a46c085d170933edbc6bc
Source dataset
uspto-grants-1999_10
Patent number
US05972957

Reaction notes

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