Benzoic Acid → 1-Phenyl-1-propanone
Reaction equation
[C:1]([OH:9])(=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:10](O)(=O)[CH2:11]C>O>[C:1]([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)(=[O:9])[CH2:10][CH3:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 16 g/h of benzoic acid, 57 g/h of propionic acid and 14.5 g/h of water was evaporated in an evaporator and passed, together with 10 l/h of nitrogen, at 400° C., over 100 ml of a catalyst which contained 2.5% by weight of sodium oxide, the remainder being anatase. The reaction gases were then cooled and were collected in a receiver. From the discharged two-phase mixture, the organic phase was analyzed by gas chromatography. The conversion of both carboxylic acids was 100%. The selectivity with respect to propiophenone was 99%.
Workup
- customwas evaporated in an evaporator
- custompassed, together with 10 l/h of nitrogen, at 400° C., over 100 ml of a catalyst which
- customThe reaction gases
- temperaturewere then cooled
- customwere collected in a receiver
Sources & evidence
- ORD record
- ord-850fbe7ba64a467aa422ae8db35bba73
- Source dataset
- uspto-grants-1990_08
- Patent number
- US04950763
Reaction notes
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