Reaction equation
CC(C)([O-])C.[K+].[CH3:7][C:8]1[N:13]=[CH:12][C:11]([OH:14])=[CH:10][CH:9]=1.[CH2:15]([O:17][C:18](=[O:23])[CH:19]=[C:20](Cl)[CH3:21])[CH3:16]>O1CCCC1>[CH2:15]([O:17][C:18](=[O:23])/[CH:19]=[C:20](/[O:14][C:11]1[CH:12]=[N:13][C:8]([CH3:7])=[CH:9][CH:10]=1)\[CH3:21])[CH3:16]Participants
Conditions
- Temperature
- 23 °C
Procedure
Potassium t-butoxide (10.4 g, 0.092 mol) was added to a stirred solution of 6-methyl-pyridin-3-ol (5.00 g, 0.046 mol) in tetrahydrofuran (35 mL) at 23° C. under nitrogen and the reaction mixture was heated to reflux for 0.75 h. The reaction mixture was cooled to 23° C. and a solution of 3-chloro-but-2-enoic acid ethyl ester (prepared as in Example 191, 6.80 g, 0.046 mol) in tetrahydrofuran (40 mL) was added to the reaction mixture. The reaction mixture was refluxed for an additional 3 h. After this time, the mixture was concentrated in vacuo and the residue was diluted with water and extracted with diethyl ether. The organic layer was then washed with 5% aqueous sodium hydroxide solution followed by a saturated aqueous sodium chloride solution, dried over sodium sulfate and concentrated in vacuo to afford (E)-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl ester (5.72 g, 56%) as a yellow oil.
Workup
- temperaturethe reaction mixture was heated
- temperatureto reflux for 0.75 h
- temperatureThe reaction mixture was refluxed for an additional 3 h
- concentrationAfter this time, the mixture was concentrated in vacuo
- additionthe residue was diluted with water
- extractionextracted with diethyl ether
- washThe organic layer was then washed with 5% aqueous sodium hydroxide solution
- dry with materialdried over sodium sulfate
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-9d2a281a183f498c80f0f0e0326b5d45
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741327B2
Linked notes
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