HCID 15541117, compound → HCID 14116663, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[CH2:15][CH2:16][C:17]([O:19]C)=[O:18])=[CH:10][CH:9]=2)=[CH:4][CH:3]=1>Cl>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[CH:13]=[CH:12][C:11]([C:14](=[O:21])[CH2:15][CH2:16][C:17]([OH:19])=[O:18])=[CH:10][CH:9]=2)=[CH:6][CH:7]=1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 4-(4′-bromo-biphenyl-4-yl)-4-oxo-butyric acid, methyl ester (2.636 g, 0.00759 mol) in 6 M HCl was refluxed for 24 hours and cooled to room temperature. The solids were filtered and washed with 1 M HCl. The filter cake was partitioned between ethyl acetate and 1 M sodium hydroxide. The aqueous layer was washed twice with ethyl acetate and filtered to remove particulates. The filtrate was rotary evaporated to remove residual ethyl acetate. The solution was stirred and acidified to pH 2 with concentrated HCl solution. The resulting precipitate was filtered, washed with water, and dried with house vacuum (air bleed) to give 1.97 g of 4-(4′-bromo-biphenyl-4-yl)-4-oxo-butyric acid as a white solid; mp 198-200° C.
Workup
- temperaturewas refluxed for 24 hours
- filtrationThe solids were filtered
- washwashed with 1 M HCl
- customThe filter cake was partitioned between ethyl acetate and 1 M sodium hydroxide
- washThe aqueous layer was washed twice with ethyl acetate
- filtrationfiltered
- customto remove particulates
- customThe filtrate was rotary evaporated
- customto remove residual ethyl acetate
- filtrationThe resulting precipitate was filtered
- washwashed with water
- customdried with house vacuum (air bleed)
Sources & evidence
- ORD record
- ord-93f0ff2163bb468db23382cfd6bdcc0d
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06239288B1
Reaction notes
Loading…