Benzaldehyde → HCID 546254, compound
Reaction equation
[CH:1](=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:9]([O:13]C(=O)CC)(=[O:12])[CH2:10][CH3:11].Cl(O)(=O)(=O)=O>>[C:1]([O:8][CH:1]([O:13][C:9](=[O:12])[CH2:10][CH3:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)(=[O:8])[CH2:2][CH3:3]Participants
4
Procedure
Benzaldehyde (1.5 mol) and propionic anhydride (1.5 mol) were reacted in the presence of 0.5 ml perchloric acid by the procedure of Example 4. The resulting benzylidene bispropionate distilled at 104° C (0.1 (mm/Hg).
Workup
- distillationThe resulting benzylidene bispropionate distilled at 104° C (0.1 (mm/Hg)
Sources & evidence
- ORD record
- ord-0fa2a3543fc94608bbb4be3ecc07e926
- Source dataset
- uspto-grants-1977_03
- Patent number
- US04012526
Reaction notes
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