Acetic Acid → HCID 21439773, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:18]=[CH:17][C:6]([CH:7]([OH:16])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:14][OH:15])=[CH:5][CH:4]=1.C(O)(=O)C.[Se](=O)=O>CC(O)C>[C:7]([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][C:9]=1[CH:14]=[O:15])(=[O:16])[C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:18][CH:17]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 26 g. of 4'-methoxy-2-hydroxymethylbenzhydrol in 140 ml. of acetic acid and 14.5 g. selenium dioxide was refluxed for 2 hours. The mixture was filtered and the filtrate was made basic. An oil separated which crystallized on standing and was collected. Recrystallization from a mixture of methylene chloride and petroleum ether gave off-white platelets melting at 90°-91°. Ultraviolet maxima (2-propanol) at 221 μ (ε = 21,600), 258 μ ε = 12,400) and 292 μ (ε = 17,000); infrared absorption (CHCl3) at 1660 cm-1 and at 1700 cm-1.
Workup
- filtrationThe mixture was filtered
- customAn oil separated which
- customcrystallized
- customwas collected
- customRecrystallization
- additionfrom a mixture of methylene chloride and petroleum ether
- customgave off-white platelets melting at 90°-91°
- customabsorption (CHCl3) at 1660 cm-1
Sources & evidence
- ORD record
- ord-9dfe56dc814249b7a7c9add0ad224295
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04018765
Reaction notes
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