Lithium Hydroxide → HCID 67393125, compound
Reaction equation
[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1/[CH:7]=[CH:8]/[C:9]1[CH:18]=[CH:17][C:12]([C:13]([O:15]C)=[O:14])=[CH:11][CH:10]=1.[OH-].[Li+:20]>CO>[Li+:20].[CH3:1][N:2]1[CH:6]=[CH:5][CH:4]=[C:3]1/[CH:7]=[CH:8]/[C:9]1[CH:10]=[CH:11][C:12]([C:13]([O-:15])=[O:14])=[CH:17][CH:18]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
Methyl 4-[(E)-2-(1-methyl-1H-pyrrol-2-yl)ethenyl]benzoate (40 mg, 0.166 mmol; see step (i) above) was suspended in a mixture of methanol (1 mL) and lithium hydroxide solution (16 mg of LiOH in water 2 mL). The reaction mixture was heated at 60° C. overnight with stirring. This solution was freeze-dried and the title compound used in the next step without further purification.
Workup
- customThis solution was freeze-dried
- customthe title compound used in the next step without further purification
Sources & evidence
- ORD record
- ord-a5f47186ec2146cfa354c6e67091b6ab
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08012967B2
Reaction notes
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