Ethyl 3-bromopentanoate → 3-hexyloxy-4-hydroxy-8-(4-ethoxycarbonylbutoxy)-2H-1-benzopyran-2-one
Reaction equation
[CH2:1]([O:7][C:8]1[C:9](=[O:20])[O:10][C:11]2[C:18]([OH:19])=[CH:17][CH:16]=[CH:15][C:12]=2[C:13]=1[OH:14])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].Br[CH:22]([CH2:29][CH3:30])[CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25]>>[CH2:1]([O:7][C:8]1[C:9](=[O:20])[O:10][C:11]2[C:18]([O:19][CH2:30][CH2:29][CH2:22][CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25])=[CH:17][CH:16]=[CH:15][C:12]=2[C:13]=1[OH:14])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]Participants
3
Procedure
In the same manner as in Reference Example 3, except that an equimolar amount of 3-hexyloxy-4,8-dihydroxy-2H-1-benzopyran-2-one was used in place of 3-hexyloxy-4,5-dihydroxy-2H-1-benzopyran-2-one, and ethyl 3-bromopentanoate was used in place of ethyl bromoacetate in Reference Example 3, 3-hexyloxy-4-hydroxy-8-(4-ethoxycarbonylbutoxy)-2H-1-benzopyran-2-one was obtained.
Sources & evidence
- ORD record
- ord-83e9aff7bd4244b197d23f30ea7b03f2
- Source dataset
- uspto-grants-2003_12
- Patent number
- US06670391B2
Reaction notes
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