Water → HCID 86208818, compound
Reaction equation
[H-].[Na+].[CH2:3]([OH:8])[CH2:4][CH2:5][CH2:6][OH:7].BrC[CH2:11][C:12]([O:14][CH3:15])=[O:13].O>C1COCC1>[CH3:15][O:14][C:12](=[O:13])[CH2:11][O:7][CH2:6][CH2:5][CH2:4][CH2:3][OH:8]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Sodium hydride (4.44 g, 60% dispersion in oil, 111 mmol) was added to a solution of 1,4-butanediol (10.0 g, 111 mmol) in THF (200 mL). After stirring 1 h at rt, the mixture was cooled to 0° C. and methyl bromomethylacetate (10.82 mL, 114 mmol) was added and the reaction was allowed to warm to room temperature. After 16 h, water (100 mL) was added and the mixture was extracted with EtOAc (3×100 mL). The combined organic phase was washed with brine (2×100 mL), dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by flash column chromatography (20%→30% EtOAc/Hexane) to afford 2.88 g (16%) of (4-hydroxy-butoxy)-acetic acid methyl ester as a colorless oil.
Workup
- temperaturethe mixture was cooled to 0° C.
- temperatureto warm to room temperature
- waitAfter 16 h
- extractionthe mixture was extracted with EtOAc (3×100 mL)
- washThe combined organic phase was washed with brine (2×100 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was purified by flash column chromatography (20%→30% EtOAc/Hexane)
Sources & evidence
- ORD record
- ord-c9ce0cdb96104d808498eccc129d5fc0
- Source dataset
- uspto-grants-2004_05
- Patent number
- US06734206B1
Reaction notes
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