Potassium Carbonate → HCID 18331486, compound
Reaction equation
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:10]2[CH:15]=[CH:14][C:13]([O:16][CH3:17])=[CH:12][C:11]=2[OH:18])=O)=[CH:4][CH:3]=1.[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([CH2:26][C:27](O)=[O:28])=[CH:22][CH:21]=1.C([O-])([O-])=O.[K+].[K+].C(N1C=CN=C1)(N1C=CN=C1)=O>CN(C)C1C=CN=CC=1.CN(C=O)C.O>[Cl:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[C:27](=[O:28])[O:18][C:11]3[C:10]([C:8]=2[C:5]2[CH:6]=[CH:7][C:2]([OH:1])=[CH:3][CH:4]=2)=[CH:15][CH:14]=[C:13]([O:16][CH3:17])[CH:12]=3)=[CH:22][CH:21]=1Participants
8
Reactant 4
Product 1
Reagents, catalysts & solvents 3
Conditions
- Temperature
- 90 °C
Procedure
A suspension of 2-hydroxy-4-methoxyphenyl 4-hydroxyphenyl ketone (2.6 grams, 10.65 mmol), 4-chlorophenylacetic acid (4.0 g, 23.43 mmol), K2CO3 (4.4 g, 31.95 mmol), carbonyldiimidazole (3.8 g, 23.43 mmol), and 4-dimethylaminopyridine (0.1 g,) in 20 mL of DMF was warmed at 90° C. for 5 hours. The reaction mixture was poured into 150 mL of H2O and stirred for 30 minutes. The precipitated product was collected by filtration and the purified desired product was isolated following flash chromatography (2.1 g, 52%, LC/MS=379 (M+H+)).
Workup
- filtrationThe precipitated product was collected by filtration
- customthe purified desired product
- customwas isolated
Sources & evidence
- ORD record
- ord-32108088900f494fa43cfbd608de22f8
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331562B1
Reaction notes
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