Diisobutylaluminumhydride → HCID 23361364, compound
Reaction equation
[CH3:1][C:2]1[S:6][C:5]([CH2:7][O:8][C:9]2[CH:20]=[CH:19][C:12]([CH:13]=[CH:14][C:15](OC)=[O:16])=[CH:11][CH:10]=2)=[N:4][C:3]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.[H-].C([Al+]CC(C)C)C(C)C>>[CH3:1][C:2]1[S:6][C:5]([CH2:7][O:8][C:9]2[CH:20]=[CH:19][C:12](/[CH:13]=[CH:14]/[CH2:15][OH:16])=[CH:11][CH:10]=2)=[N:4][C:3]=1[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1Participants
3
Procedure
According to the method described for Reference Example 23, methyl 4-(5-methyl-4-phenyl-2-thiazolylmethoxy)cinnamate was subjected to reduction with diisobutylaluminum hydride to give (E)-3-[4-(5-methyl-4-phenyl-2-thiazolylmethoxy)phenyl]-2-propen-1-ol. Recrystallization from ethyl acetate--isopropyl ether gave colorless prisms, m.p.125°-126° C.
Sources & evidence
- ORD record
- ord-86e073275bc447b1a9f53d1df6953e82
- Source dataset
- uspto-grants-1997_01
- Patent number
- US05591862
Reaction notes
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