4-Hydroxy-2-methylacetophenone → HCID 178466794, compound

HRID 1067710Notes

Reaction equation

HRID 1067710 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][OH:16])[N:10]=[CH:9]2)C=CC=CC=1.O[C:30]1[CH:35]=[CH:34][C:33]([C:36](=[O:38])[CH3:37])=[C:32]([CH3:39])[CH:31]=1>>[NH:8]1[CH:12]=[C:11]([CH2:13][CH2:14][CH2:15][O:16][C:30]2[CH:35]=[CH:34][C:33]([C:36](=[O:38])[CH3:37])=[C:32]([CH3:39])[CH:31]=2)[N:10]=[CH:9]1

Participants

3

Reactant 2

HCID 701334-Hydroxy-2-methylacetophenoneHCID 108328403-(1-Trityl-1H-imidazol-4-YL)propan-1-OL

Product 1

HCID 178466794HCID 178466794, compound

Procedure

5 mmol of 3-(1-triphenylmethyl-1H-imidazol-4-yl)propanol and 6 mmol of (4-hydroxy-2-methylphenyl)ethanone are treated as described in Example 56, but isolated in the form of the free base.

Workup

  1. customisolated in the form of the free base

Sources & evidence

ORD record
ord-11ae878c49fd4d2b886cbd859c26a4c5
Source dataset
uspto-grants-2001_06
Patent number
US06248765B1

Reaction notes

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