Water → 2-(Oxan-4-yloxy)acetic acid
Reaction equation
[O:1]1[CH2:6][CH2:5][CH:4]([OH:7])[CH2:3][CH2:2]1.I[CH2:9][C:10]([O-:12])=[O:11].[Na+].[H-].[Na+].O>O1CCCC1>[O:1]1[CH2:6][CH2:5][CH:4]([O:7][CH2:9][C:10]([OH:12])=[O:11])[CH2:3][CH2:2]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A solution of tetrahydro-2H-pyran-4-ol (286 μl, Acros) in tetrahydrofuran (4 ml) was added with sodium iodoacetate (624 mg), and successively added with sodium hydride (198 mg) as several portions at 0° C., and the mixture was stirred at the same temperature for 45 minutes, and then further stirred at room temperature for 23 hours. The reaction mixture was cooled again to 0° C., and then carefully added with water and then with chloroform, and the organic layer was separated. The aqueous layer was acidified (pH 4) with 1 N hydrochloric acid, and extracted three times with chloroform, and the combined organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated under reduced pressure to obtain the title compound (43.4 mg).
Workup
- stirringfurther stirred at room temperature for 23 hours
- customwith chloroform, and the organic layer was separated
- extractionextracted three times with chloroform
- washthe combined organic layer was washed with saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThen, the solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-bcf3306df9a64933b77dced4cae87e88
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964613B2
Reaction notes
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