diethyl 3,4-dihydro-7-[3-(4-chlorophenoxy)propoxy]-4-oxo-8-propyl-2H-1-benzopyran-2,2-dipropanoate → 3,4-dihydro-4-oxo-7-(3-phenoxypropoxy)-2H-1-benzopyran-2,2-dipropanoic acid
Reaction equation
[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][C:10]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11][C:6]=2[O:5][C:4]([CH2:30][CH2:31][C:32]([O:34]CC)=[O:33])([CH2:23][CH2:24][C:25]([O:27]CC)=[O:26])[CH2:3]1.ClC1C=CC(OCCCOC2C=CC3C(=O)CC(CCC(OCC)=O)(CCC(OCC)=O)OC=3C=2CCC)=CC=1>>[O:1]=[C:2]1[C:7]2[CH:8]=[CH:9][C:10]([O:12][CH2:13][CH2:14][CH2:15][O:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[CH:11][C:6]=2[O:5][C:4]([CH2:23][CH2:24][C:25]([OH:27])=[O:26])([CH2:30][CH2:31][C:32]([OH:34])=[O:33])[CH2:3]1Participants
3
Reactant 2
Product 1
Procedure
The title compound was prepared by the method of Example 22 substituting the title product of Example 26 for the title product of Example 21. Crystallization from 60% by volume ethyl acetate/hexane yielded 219 mg, m.p. 132°-133° C.
Workup
- customCrystallization from 60% by volume ethyl acetate/hexane
- customyielded 219 mg, m.p. 132°-133° C.
Sources & evidence
- ORD record
- ord-78de87d996f14ec4913e4a4f61a44440
- Source dataset
- uspto-grants-1992_03
- Patent number
- US05093353
Reaction notes
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