4-Hydroxyphenylacetone → HCID 178467618, compound
Reaction equation
C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)[N:8]2[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15]O)[N:10]=[CH:9]2)C=CC=CC=1.[OH:29][C:30]1[CH:35]=[CH:34][C:33]([CH2:36][C:37](=[O:39])[CH3:38])=[CH:32][CH:31]=1>>[NH:8]1[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O:29][C:30]2[CH:31]=[CH:32][C:33]([CH2:36][C:37](=[O:39])[CH3:38])=[CH:34][CH:35]=2)[N:10]=[CH:9]1Participants
3
Procedure
5 mmol of 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanol and 6 mmol of 4-hydroxyphenylpropanone are treated as described in Example 76.
Sources & evidence
- ORD record
- ord-3f9738c8a7cd493f9ccf41f49e83480a
- Source dataset
- uspto-grants-2001_06
- Patent number
- US06248765B1
Reaction notes
Loading…