Water → 1,1-Dimethylethyl 2-(3-pyridinylmethoxy)acetate

HRID 2112358Notes

Reaction equation

HRID 2112358 reaction equation
[H-].[Na+].[N:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH2:9][OH:10])[CH:4]=1.Br[CH:12](C)[C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14].O>C1COCC1>[N:3]1[CH:8]=[CH:7][CH:6]=[C:5]([CH2:9][O:10][CH2:12][C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH:4]=1

Participants

6

Reactant 4

HCID 962WaterHCID 75103-PyridinemethanolHCID 24758Sodium hydrideHCID 545327tert-Butyl 2-bromopropanoate

Product 1

HCID 247635281,1-Dimethylethyl 2-(3-pyridinylmethoxy)acetateYield 59.9%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent3×

Procedure

To a suspension of 1.24 g of sodium hydride (60% oil dispersion; 31 mmol) in 90 mL of THF were added dropwise 3.27 g of 3-pyridinemethanol (30 mmol) in 10 mL of dry THF at room temperature over 5 min. The resulting white suspension was stirred at room temperature for an hour, to which was then added dropwise 6.27 g of tert-butyl 2-bromopropionate (30 mmol) in 10 mL of dry THF at room temperature over 5 min. The mixture was stirred at room temperature for 11.5 hours. After adding water, the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried and evaporated. The residue was purified by column chromatography on silica gel (eluent: n-hexane:ethyl acetate=1:1) to give 4.01 g of tert-butyl (pyridin-3-yl)methoxyacetate (Yield: 56.3%) as a dark brown oil.

Workup

  1. stirringThe mixture was stirred at room temperature for 11.5 hours
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with saturated brine
  4. customdried
  5. customevaporated
  6. customThe residue was purified by column chromatography on silica gel (eluent: n-hexane:ethyl acetate=1:1)

Sources & evidence

ORD record
ord-ed8fb1b6ca2245d5839cb96e833b06a6
Source dataset
uspto-grants-2009_04
Patent number
USRE040703E1

Reaction notes

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