Reaction equation
[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([C:10]([O:12]CC)=[O:11])[C:5]([CH3:15])=[C:4]([CH3:16])[C:3]=1[C:17](=[O:35])[CH:18]=[CH:19][C:20]1C=C(C(C)(C)C)[C:23](O)=[C:22]([C:31](C)(C)C)[CH:21]=1.CC1C=CC(C=[S:42])=CC=1>>[OH:1][C:2]1[C:7]([O:8][CH3:9])=[C:6]([C:10]([OH:12])=[O:11])[C:5]([CH3:15])=[C:4]([CH3:16])[C:3]=1[C:17](=[O:35])[CH:18]=[CH:19][C:20]1[S:42][CH:23]=[C:22]([CH3:31])[CH:21]=1Participants
3
Procedure
This compound was synthesized from 2′-hydroxy-4′-ethyloxycarbonyldimethylmethyloxyacetophenone (starting material 1) and 4-methylthiobenzaldehyde according to general method 2 described earlier.
Sources & evidence
- ORD record
- ord-9ba8fa96bbab4ab5a3f15d0c5b7f4fb2
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08058308B2
Linked notes
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