Potassium Iodide → HCID 54082516, compound

HRID 1580732Notes

Reaction equation

HRID 1580732 reaction equation
C(=O)([O-])[O-].[K+].[K+].[I-].[K+].Br[CH2:10][CH2:11][CH:12]=[C:13]([CH3:20])[CH2:14][CH2:15][O:16][CH:17]([CH3:19])[CH3:18].[CH2:21]1[O:29][C:28]2[CH:27]=[CH:26][C:25]([OH:30])=[CH:24][C:23]=2[O:22]1>CC(C)=O>[CH:17]([O:16][CH2:15][CH2:14][C:13]([CH3:20])=[CH:12][CH2:11][CH2:10][O:30][C:25]1[CH:26]=[CH:27][C:28]2[O:29][CH2:21][O:22][C:23]=2[CH:24]=1)([CH3:19])[CH3:18]

Participants

6

Procedure

2.35 g (0.017 mol) of potassium carbonate and 50 mg of potassium iodide are added to a solution of 4.0 g (0.017 mol) of 1-bromo-6-isopropoxy-4-methyl-3-hexene and 2.35 g (0.017 mol) of 3,4-methylendioxy-phenol in 120 cc of acetone. The suspension is boiled under reflux during the course of 20 hours, is then filtered and liberated from acetone in a vacuum. The residue is taken up in ether, washed with water and saturated salt solution, dried over sodium sulphate and evaporated. The residue is chromatographed on silica gel with hexane/ethyl acetate 9 : 1. Thus the cis/trans isomeric mixture of the 5-(6-isopropoxy-4-methyl methyl-3-hexenyloxy)-1,3-benzodioxol is obtained as colourless oil. nD20 = 1.5111.

Workup

  1. temperatureunder reflux during the course of 20 hours
  2. filtrationis then filtered
  3. washwashed with water and saturated salt solution
  4. dry with materialdried over sodium sulphate
  5. customevaporated
  6. customThe residue is chromatographed on silica gel with hexane/ethyl acetate 9 : 1
  7. additionThus the cis/trans isomeric mixture of the 5-(6-isopropoxy-4-methyl methyl-3-hexenyloxy)-1,3-benzodioxol
  8. customis obtained as colourless oil

Sources & evidence

ORD record
ord-58ae4879a7324628aa2371da2ad9ff91
Source dataset
uspto-grants-1976_01
Patent number
US03933804

Reaction notes

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