Water → HCID 57681491, compound
Reaction equation
Br[C:2]([CH2:26][CH3:27])([CH2:24][CH3:25])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18](=[O:23])[C:19](Br)([CH3:21])[CH3:20])=[CH:14][CH:13]=2)=[CH:7][CH:6]=1)=[O:4].[OH-:28].[Na+].[OH2:30]>ClCCl.CC[N+](CC1C=CC=CC=1)(CC)CC.[Cl-]>[CH2:24]([C:2]([OH:30])([CH2:26][CH3:27])[C:3]([C:5]1[CH:10]=[CH:9][C:8]([O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18](=[O:23])[C:19]([OH:28])([CH3:21])[CH3:20])=[CH:14][CH:13]=2)=[CH:7][CH:6]=1)=[O:4])[CH3:25]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 29.15 g (0.0587 mol) of 2-bromo-1-{4-[4-(2-bromo-2-methyl-propionyl)-phenoxy]-phenyl}-2-ethyl-butane-1-one dissolved in 60 ml of dichloromethane, 16.88 g (0.211 mol) of 50% NaOH and 291.5 mg of 50% BTEAC were added. The reaction was refluxed for 3 h, adding every 30′, 291.5 mg of BTEAC, then diluted with water and dichloromethane.
Workup
- temperatureThe reaction was refluxed for 3 h
Sources & evidence
- ORD record
- ord-297892acd2e148c2836bf05eeb225c8e
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07534880B2
Reaction notes
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