Potassium Hydroxide → HCID 14515745, compound

HRID 1723191Notes

Reaction equation

HRID 1723191 reaction equation
[CH3:1][C:2](N(C)C)=[O:3].[CH:7]([C:10]1[CH:19]=[CH:18][CH:17]=[C:16]2[C:12](=[CH:13][CH:14]=[CH:15]2)[CH:11]=1)([CH3:9])[CH3:8].P(Cl)(Cl)(Cl)=O.[OH-].[K+]>O>[C:2]([C:13]1[C:12]2[C:16]([CH:17]=[CH:18][CH:19]=[C:10]([CH:7]([CH3:9])[CH3:8])[CH:11]=2)=[CH:15][CH:14]=1)(=[O:3])[CH3:1]

Participants

6

Procedure

To a dimethylacetamide (80 ml) solution of the compound (19) (8.41 g), while stirring and cooling with ice. a dimethylacetamide (76 ml) solution of phosphorus oxychloride (POC13) (92 g) was added dropwise over 40 minutes. After the addition of the POC13 solution, it was further stirred for 5 hours at room temperature, and then poured into water (800 ml). The solution was made basic (pH 10) by the addition of aqueous potassium hydroxide, and was extracted 5 times with benzene. The benzene solutions were mixed, washed with water and dried. From the benzene solution, the solvent was distilled off to obtain an oily substance. It was purified by silica gel column chromatography (650 g), eluting with benzene. The secondeluted part gave 1-acetyl-7-isopropylazulene (20) (4.29 g, 41%) in a red oily state.

Workup

  1. temperaturecooling with ice
  2. additionAfter the addition of the POC13 solution, it
  3. extractionwas extracted 5 times with benzene
  4. additionThe benzene solutions were mixed
  5. washwashed with water
  6. customdried
  7. distillationFrom the benzene solution, the solvent was distilled off
  8. customto obtain an oily substance
  9. customIt was purified by silica gel column chromatography (650 g)
  10. washeluting with benzene

Sources & evidence

ORD record
ord-b6ec3c61e591450d965803e8e0fa5f93
Source dataset
uspto-grants-1989_08
Patent number
US04859701

Reaction notes

Loading…