Methanol → HCID 86733540, compound
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
- additionA mixture of 3.60 g
- customThe resulting mixture was flushed with nitrogen
- customto come to 0°C.
- addition(39 mm.) of dimethyl sulfide were added
- additiona suspension of 1.47 g
- additionof absolute ethanol was added dropwise
- customto come up to room temperature
- stirringstirred for 80 minutes
- customThe methanol was removed under vacuum
- customto produce 3.54 g
- 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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