Methanol → HCID 86733540, compound

HRID 1657972Notes

Reaction equation

HRID 1657972 reaction equation
[CH:1]([O:4][C:5]1C[CH:9]=[CH:8][CH2:7][CH:6]=1)([CH3:3])[CH3:2].[O:11]=[O+][O-].[CH3:14][OH:15]>>[OH:15][CH2:14][CH2:9]/[CH:8]=[CH:7]\[CH2:6][C:5]([O:4][CH:1]([CH3:3])[CH3:2])=[O:11]

Participants

4

Conditions

Temperature
-78 °C

Procedure

A mixture of 3.60 g. (26 mm.) of 1-isopropoxy-1,4-cyclohexadiene and 100 ml. of absolute methanol was treated with ozone (1.25 g., 26 mm.) at -78°C. The resulting mixture was flushed with nitrogen. The mixture was allowed to come to 0°C. and 2.42 g. (39 mm.) of dimethyl sulfide were added and the mixture stirred at this temperature for 80 minutes. After cooling to -78°C, a suspension of 1.47 g. (39 mm.) of sodium borohydride in 20 ml. of absolute ethanol was added dropwise. The resulting mixture was allowed to come up to room temperature and then stirred for 80 minutes. The methanol was removed under vacuum to produce 3.54 g. of product (80% of theory), b.p. 72° (0.2 mm., short path distillation).

Workup

  1. additionA mixture of 3.60 g
  2. customThe resulting mixture was flushed with nitrogen
  3. customto come to 0°C.
  4. addition(39 mm.) of dimethyl sulfide were added
  5. additiona suspension of 1.47 g
  6. additionof absolute ethanol was added dropwise
  7. customto come up to room temperature
  8. stirringstirred for 80 minutes
  9. customThe methanol was removed under vacuum
  10. customto produce 3.54 g
  11. distillationof product (80% of theory), b.p. 72° (0.2 mm., short path distillation)

Sources & evidence

ORD record
ord-ee3df6f592c3459e99df76c65a7a7a35
Source dataset
uspto-grants-1976_06
Patent number
US03962354

Reaction notes

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