HCID 13290642, compound → 5-Benzyl-4-hydroxymethyloxazole
Reaction equation
[CH2:1]([C:8]1[O:12][CH:11]=[N:10][C:9]=1[C:13](OC)=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH2:1]([C:8]1[O:12][CH:11]=[N:10][C:9]=1[CH2:13][OH:14])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Methyl 5-benzyl-4-oxazolecarboxylate is reduced with lithium aluminium hydride in tetrahydrofuran to give 5-benzyl-4-hydroxymethyloxazole, which on reaction with thionyl chloride is converted to 5-benzyl-4-chloromethyl-oxazole.
Sources & evidence
- ORD record
- ord-0498e780b3344e4ba0c68c63a7136e70
- Source dataset
- uspto-grants-1978_01
- Patent number
- US04069327
Reaction notes
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