Lithium Hydroxide → HCID 23714172, compound
Reaction equation
[C:1]1([C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][N:16]=2)[C:10]([O:12]C)=[O:11])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Li+:18]>C1COCC1>[C:1]1([C:7]2[CH:8]=[C:9]([CH:14]=[CH:15][N:16]=2)[C:10]([O-:12])=[O:11])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1.[Li+:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Preparation H1, Step 4: A solution of methyl 2-phenylisonicotinate, N-oxide (397 mg, 1.73 mmol) in THF (6 mL) was treated with 0.5 N aqueous lithium hydroxide (3.65 mL, 1.81 mmol), and the mixture was stirred overnight. The THF was stripped, and the aqueous solution was freeze dried to yield lithium 2-phenylisonicotinate, N-oxide a colorless glass, which was used as-is in the next step.
Workup
- customPreparation H1, Step 4
- customdried
Sources & evidence
- ORD record
- ord-5e703eadbef24052b51cada966641cc9
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07378409B2
Reaction notes
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