Reaction equation
[CH3:1][O:2][C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([O:10]C)=[O:9].[OH-].[Na+].Cl>C1COCC1>[CH3:1][O:2][C:3]1[CH:7]=[CH:6][S:5][C:4]=1[C:8]([OH:10])=[O:9]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 75 °C
Procedure
To a solution of methyl 3-methoxythiophene carboxylate (2.0 g, 11.6 mmol) in 20 mL of THF at room temperature was added dropwise a 1.0 M sodium hydroxide aqueous solution (17.0 mL, 17.0 mmol). After addition, the mixture was heated to 75° C. (oil bath temperature) and continued for 18 h. The mixture was cooled to room temperature, treated with a 1.0 M hydrochloride aqueous solution until pH approximately being 2. The acidified mixture was extracted with 100 mL of CH2Cl2—CH3CN (1:1, v/v), 50 mL of CH2Cl2, and 50 mL of CH3CN. The combined organic extracts were washed with brine (30 mL), dried over Na2SO4, and concentrated under reduced pressure to a solid, which was further dried on high vacuum, yielding 1.84 g (100%) of 3-methoxythiophene carboxylic acid (MH+=159.0).
Workup
- additionAfter addition
- temperatureThe mixture was cooled to room temperature
- extractionThe acidified mixture was extracted with 100 mL of CH2Cl2—CH3CN (1:1
- washThe combined organic extracts were washed with brine (30 mL)
- dry with materialdried over Na2SO4
- concentrationconcentrated under reduced pressure to a solid, which
- customwas further dried on high vacuum
Sources & evidence
- ORD record
- ord-8a82f5a4e7034b07b5125a10dc692519
- Source dataset
- uspto-grants-2005_04
- Patent number
- US06878709B2
Linked notes
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