Phthalic Anhydride → 2-(1-Hydroxypentan-2-yl)isoindoline-1,3-dione
Reaction equation
[C:1]1(=[O:11])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3](=[O:10])O1.[NH2:12][CH:13]([CH2:16][CH2:17][CH3:18])[CH2:14][OH:15]>>[OH:15][CH2:14][CH:13]([N:12]1[C:3](=[O:10])[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[C:1]1=[O:11])[CH2:16][CH2:17][CH3:18]Participants
3
Procedure
2-(1-hydroxypentan-2-yl)isoindoline-1,3-dione was prepared in a similar manner to example 9c using isobenzofuran-1,3-dione and 2-aminopentan-1-ol. Yield 62%.
Sources & evidence
- ORD record
- ord-da9ce0894a65498fa50b6577cb070ceb
- Source dataset
- uspto-grants-2009_01
- Patent number
- US07476399B2
Reaction notes
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