Furfural → [2-(Furan-2-yl)-4-phenyl-1,3-dioxolan-4-yl](phenyl)methanone
Reaction equation
[CH2:1]([C:3]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([OH:12])[C:4](=[O:11])[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1)[OH:2].[CH:19](=O)[C:20]1[O:24][CH:23]=[CH:22][CH:21]=1>>[O:24]1[CH:23]=[CH:22][CH:21]=[C:20]1[CH:19]1[O:12][C:3]([C:4](=[O:11])[C:5]2[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=2)([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:1][O:2]1Participants
3
Procedure
The procedure of Example 1 was repeated except that the starting materials were α-methylolbenzoin and furfural. The product 2-furyl-4-benzoyl-4-phenyl-1,3-dioxolane, was obtained in a yield of 78% and analyzed as follows:
Sources & evidence
- ORD record
- ord-7ce6625966e3430db1417f5823cc3436
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03944509
Reaction notes
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