1,1-Dimethoxy-2-methyl-2-acetoxy-but-3-ene → 4,4-Dimethoxy-3-methyl-crotyl acetate

HRID 1155269Notes

Reaction equation

HRID 1155269 reaction equation
[CH3:1][O:2][CH:3]([O:12][CH3:13])[C:4]([CH3:11])(OC(=O)C)[CH:5]=[CH2:6]>[Cu]Cl>[C:3]([O:12][CH2:6][CH:5]=[C:4]([CH3:11])[CH:3]([O:2][CH3:1])[O:12][CH3:13])(=[O:2])[CH3:4]

Participants

3

Conditions

Temperature
147 °C

Procedure

564 parts of 1,1-dimethoxy-2-methyl-2-acetoxy-but-3-ene and 0.3 parts of copper (I) chloride were heated, with stirring, at 147° C., under a pressure of 0.2 bar, in a reaction vessel equipped with a stirrer, an internal thermometer, and a descending condenser. During the reaction time of 7.5 hours, the low-boiling products formed distilled off continuously and the reaction temperature rose to 157° C. Subsequent working up of the reaction mixture by distillation gave 459 parts of 4,4-dimethoxy-3-methyl-crotyl acetate, corresponding to a yield of 81.4% of theory.

Workup

  1. customequipped with a stirrer
  2. customDuring the reaction time of 7.5 hours, the low-boiling products formed
  3. distillationdistilled off continuously
  4. customrose to 157° C
  5. distillationSubsequent working up of the reaction mixture by distillation

Sources & evidence

ORD record
ord-d8e626cbd5704305b537c6f887684c22
Source dataset
uspto-grants-1981_11
Patent number
US04301084

Reaction notes

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