1,1,1-Trimethoxypropane → 1,5-Diacetyl-3-(1-methoxy-propylidene)-2-indolinone
Reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[C:17](OC)(OC)([O:20][CH3:21])[CH2:18][CH3:19]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:17]([O:20][CH3:21])[CH2:18][CH3:19])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and trimethyl orthopropionate
Sources & evidence
- ORD record
- ord-e15cfda396b94308944b844bd555b60d
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176231B2
Reaction notes
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