Dihydroxyacetone → HCID 25214745, compound
Reaction equation
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:17]=[CH:16][C:13]([CH:14]=[O:15])=[CH:12][CH:11]=1.[OH:18][CH2:19][C:20]([CH2:22][OH:23])=[O:21]>>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[CH:17]=[CH:16][C:13]([CH:14]([OH:15])[CH:19]([OH:18])[C:20](=[O:21])[CH2:22][OH:23])=[CH:12][CH:11]=1Participants
3
Procedure
Compound B was prepared as a mixture of isomers in analogy to example 1 from 4-benzoxazol-2-yl-benzaldehyde and 1,3-dihydroxyacetone.
Sources & evidence
- ORD record
- ord-3a09fd6dfb6f46f18d7d71a5a0ca9aa1
- Source dataset
- uspto-grants-2012_10
- Patent number
- US08278459B2
Reaction notes
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