Potassium Hydroxide → HCID 67020061, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]2[O:14][C:15]([CH3:23])([CH3:22])[CH2:16][CH:17]([C:18]([O:20]C)=[O:19])[C:11]2=[CH:10][C:9]=1[C:24]1[CH:29]=[CH:28][C:27]([Cl:30])=[CH:26][CH:25]=1.[OH-].[K+]>C1COCC1.CCOC(C)=O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[N:13]=[C:12]2[O:14][C:15]([CH3:23])([CH3:22])[CH2:16][CH:17]([C:18]([OH:20])=[O:19])[C:11]2=[CH:10][C:9]=1[C:24]1[CH:25]=[CH:26][C:27]([Cl:30])=[CH:28][CH:29]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 70 °C
Procedure
Product from Step A (66 mg, 0.14 mmol) was dissolved in THF (1 mL) and 10% KOH (1 mL) was added. The reaction was heated to 70° C. for 1 hr. The reaction was diluted with EtOAc and washed with 10% NaHSO4. The organic layer was separated, dried (Na2SO4), filtered and concentrated and used without any further purification
Workup
- washwashed with 10% NaHSO4
- customThe organic layer was separated
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customused without any further purification
Sources & evidence
- ORD record
- ord-7335f6b1f5564b859d1f30f37517659c
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07999107B2
Reaction notes
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