Aluminium lithium hydride → 5-[(3-Methyl-3-oxetanyl)methoxy]-1,3-benzenedimethanol
Reaction equation
[CH3:1][C:2]1([CH2:6][O:7][C:8]2[CH:9]=[C:10]([C:18](OC)=[O:19])[CH:11]=[C:12]([CH:17]=2)[C:13](OC)=[O:14])[CH2:5][O:4][CH2:3]1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH3:1][C:2]1([CH2:6][O:7][C:8]2[CH:17]=[C:12]([CH2:13][OH:14])[CH:11]=[C:10]([CH2:18][OH:19])[CH:9]=2)[CH2:5][O:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound is prepared from dimethyl 5-((3-methyloxetan-3-yl)methoxy)isophthalate by reduction with lithium aluminum hydride in tetrahydrofuran. LC (method 7): tR=0.69 min; Mass spectrum (ESI+): m/z=239 [M+H]+.
Sources & evidence
- ORD record
- ord-1dd14025886d46be84e5b54883a36f74
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642585B2
Reaction notes
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