Benzene → Butanal, 4-(acetyloxy)-2-methylene-

HRID 1703503Notes

Reaction equation

HRID 1703503 reaction equation
C([O:4][CH2:5][CH:6]=[CH:7][CH2:8][O:9][C:10](=[O:12])[CH3:11])(=O)C.[CH:13]1C=CC=CC=1>[Rh].C1(OP(OC2C=CC=CC=2)OC2C=CC=CC=2)C=CC=CC=1>[CH:5]([C:6]([CH2:7][CH2:8][O:9][C:10](=[O:12])[CH3:11])=[CH2:13])=[O:4]

Participants

5

Conditions

Temperature
85 °C

Procedure

A mixture of 1,4-diacetoxy-2-butene (170 g.), triphenylphosphite (0.51 g.), 5% rhodium on charcoal (1.12 g.) and benzene (340 g.) was loaded into a 1 liter stainless steel autoclave and heated with stirring to 85° C. The autoclave was then pressured to 2000 psig with synthesis gas. When gas uptake had ceased (approximately 3 hours), the autoclave was cooled to room temperature and vented. The reaction mixture was filtered and heated under vacuum until all the benzene had been removed. After the addition of p-toluenesulphonic acid (0.5 g.), the reaction product was heated in an oil bath at 105°-110° C. under a vacuum of 5 mm Hg. and the distillate so produced was collected and then fractionally distilled to give 2-formyl-4-acetoxybutene (126.3 g., 90% yield, b.p. 67°-72° C./ 6 mm Hg.).

Workup

  1. temperatureheated
  2. customThe autoclave was then pressured to 2000 psig with synthesis gas
  3. custom(approximately 3 hours)
  4. temperaturethe autoclave was cooled to room temperature
  5. filtrationThe reaction mixture was filtered
  6. temperatureheated under vacuum until all the benzene
  7. customhad been removed
  8. additionAfter the addition of p-toluenesulphonic acid (0.5 g.)
  9. temperaturethe reaction product was heated in an oil bath at 105°-110° C. under a vacuum of 5 mm Hg
  10. customand the distillate so produced
  11. customwas collected
  12. distillationfractionally distilled

Sources & evidence

ORD record
ord-316db8626f574e1692347d8b867211a8
Source dataset
uspto-grants-1978_11
Patent number
US04124619

Reaction notes

Loading…