Reaction equation
[C:1]1([CH2:7][N:8]2[CH:12]=[N:11][CH:10]=[N:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:13](=[O:15])[CH3:14]>>[CH2:7]([N:8]1[C:12]([CH:13]([OH:15])[CH3:14])=[N:11][CH:10]=[N:9]1)[C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1Participants
3
Procedure
1-(1-Benzyl-1H-1,2,4-triazol-5-yl)ethanol was synthesized in a manner similar to that of procedure 21B but using 1-(phenylmethyl)-1H-1,2,4-triazole and acetaldehyde as the starting materials. The product was isolated as a white solid in 86% yield.
Workup
- customThe product was isolated as a white solid in 86% yield
Sources & evidence
- ORD record
- ord-2b3bebd0777e4080b0e535de8b9c4cee
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07674813B2
Linked notes
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