Hydrogen iodide → HCID 22390446, compound

HRID 1018812Notes

Reaction equation

HRID 1018812 reaction equation
I.[Cl:2][C:3]1[CH:8]=[C:7]([C:9]2(O)[CH2:14][CH2:13][C:12]([CH3:16])([CH3:15])[CH2:11][CH2:10]2)[CH:6]=[CH:5][C:4]=1[OH:18]>C(O)(=O)C>[Cl:2][C:3]1[CH:8]=[C:7]([CH:9]2[CH2:10][CH2:11][C:12]([CH3:15])([CH3:16])[CH2:13][CH2:14]2)[CH:6]=[CH:5][C:4]=1[OH:18]

Participants

4

Procedure

50 1 of aqueous 57% hydriodic acid solution are added to 11.8 g of 2-chloro-4-(1-hydroxy-4,4-dimethylcyclohexyl)phenol in 200 ml of acetic acid. The reaction mixture is refluxed for 3 hours and the solvents are evaporated off under reduced pressure. Aqueous 40% sodium hydroxide solution, aqueous sodium carbonate solution and then aqueous sodium hydrogen sulphate solution are added and the resulting mixture is extracted with diethyl ether. The organic phase is dried over magnesium sulphate and the solvents are evaporated off under reduced pressure. The compound obtained is purified by chromatography on a column of silica gel, eluting with a 95/5 (v/v) cyclohexane/ethyl acetate mixture.

Workup

  1. temperatureThe reaction mixture is refluxed for 3 hours
  2. customthe solvents are evaporated off under reduced pressure
  3. additionAqueous 40% sodium hydroxide solution, aqueous sodium carbonate solution and then aqueous sodium hydrogen sulphate solution are added
  4. extractionthe resulting mixture is extracted with diethyl ether
  5. dry with materialThe organic phase is dried over magnesium sulphate
  6. customthe solvents are evaporated off under reduced pressure
  7. customThe compound obtained
  8. customis purified by chromatography on a column of silica gel
  9. washeluting with a 95/5 (v/v) cyclohexane/ethyl acetate mixture

Sources & evidence

ORD record
ord-cb7358e106914a5995683310d60d3a62
Source dataset
uspto-grants-2002_11
Patent number
US06482986B1

Reaction notes

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