HCID 54460329, compound → HCID 53946767, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH:17]=[CH:18][CH2:19][CH2:20]I)=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:22][C:23](=[O:28])[CH2:24][C:25](=[O:27])[CH3:26].[Li]>>[CH2:1]([O:8][C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH:17]=[CH:18][CH2:19][CH2:20][CH:24]([C:23](=[O:28])[CH3:22])[C:25](=[O:27])[CH3:26])=[CH:11][CH:10]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
[I; Ar is 3-C6H5CH2OC6H4, R0 is H, R' and R" are CH3CO, Y is CH=CHCH2CH2 ] was prepared by reacting 6-(4-benzyloxyphenyl)-3-hexenyl iodide (Preparation D16) with lithium pentane-2,4-dione. The product was chromatographed on activated magnesium silicate and eluted with benzene.
Workup
- customwas prepared
- customThe product was chromatographed on activated magnesium silicate
- washeluted with benzene
Sources & evidence
- ORD record
- ord-3e6670f0f42e45a1acd816bb8abbbc27
- Source dataset
- uspto-grants-1978_06
- Patent number
- US04093736
Reaction notes
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