Methane → 55023-57-9

HRID 1730447Notes

Reaction equation

HRID 1730447 reaction equation
[CH:1]([CH:4]([CH2:10][CH2:11][C:12](=[O:14])[CH3:13])[CH:5]=[CH:6][C:7](=[O:9])[CH3:8])([CH3:3])[CH3:2].C>[Pd].C(OCC)(=O)C>[CH:1]([CH:4]([CH2:5][CH2:6][C:7](=[O:9])[CH3:8])[CH2:10][CH2:11][C:12](=[O:14])[CH3:13])([CH3:3])[CH3:2]

Participants

5

Procedure

1.96 g (10 mM) of 5-isopropyl-non-3-ene-2,8-dione, prepared according to the method described in paragraph a) of example 2, in 20 ethyl acetate were reduced by catalytic hydrogenation in the presence of 0.196 g of palladium at 10 % over charcoal. After filtration and evaporation of the volatile portions, a residue was obtained which by fractional distillation gave 1.77 g (89 %), of the desired dione; B.p. 80°/0.001 Torr; d420 = 0.9292; nD20 = 1.4501

Workup

  1. filtrationAfter filtration and evaporation of the volatile portions
  2. customa residue was obtained which
  3. distillationby fractional distillation
  4. customgave 1.77 g (89 %)

Sources & evidence

ORD record
ord-57209e83f998452c9a7b5f4a792bf308
Source dataset
uspto-grants-1976_11
Patent number
US03992458

Reaction notes

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