Lithium Hydroxide → 3-(6-Bromopyridin-3-yl)prop-2-enoic acid
Reaction equation
C[O:2][C:3](=[O:13])[CH:4]=[CH:5][C:6]1[CH:7]=[N:8][C:9]([Br:12])=[CH:10][CH:11]=1.[Li+].[OH-]>C1COCC1.O>[Br:12][C:9]1[N:8]=[CH:7][C:6]([CH:5]=[CH:4][C:3]([OH:13])=[O:2])=[CH:11][CH:10]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To 3-(6-bromo-pyridin-3-yl)-acrylic acid methyl ester (120 mg, 0.495 mmol) in THF was added a solution of 0.5 N-LiOH (2 eq) and the mixture was stirred for 3 hrs at room temperature. The resulting residue was dissolved in H2O, then washed three times with Et2O, and neutralized with 1N HCl to pH 5˜7. The resulting solid filtered and washed with H2O and then dried in vacuo to give 3-(6-bromo-pyridin-3-yl)-acrylic acid (100 mg, 88%).
Workup
- washwashed three times with Et2O
- filtrationThe resulting solid filtered
- washwashed with H2O
- customdried in vacuo
Sources & evidence
- ORD record
- ord-8a718329b5414d23adc206f7998db42c
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858621B2
Reaction notes
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