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Sodium Acetate → Acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl ester

HRID 33565
Notes
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Reaction equation

HRID 33565 reaction equation
Br[CH2:2][C:3]([C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[CH:7][C:6]=1[O:15][CH2:16][CH3:17])=[O:4].[C:18]([O-:21])(=[O:20])[CH3:19].[Na+]>CN(C)C=O>[CH2:16]([O:15][C:6]1[CH:7]=[CH:8][C:9]2[C:14](=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:5]=1[C:3](=[O:4])[CH2:2][O:21][C:18](=[O:20])[CH3:19])[CH3:17]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 517045Sodium AcetateHCID 574553042-Bromo-1-(2-ethoxy-naphthalen-1-yl)-ethanone

Product 1

HCID 59796828Acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl esterYield 94%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent2×

Conditions

Temperature
80 °C

Procedure

A mixture of 2-bromo-1-(2-ethoxy-naphthalen-1-yl)-ethanone (7.0 g), sodium acetate (2.0 g) and N,N-dimethylformamide (80 mL) was heated at 80° C. for 1.5 hours. After cooling to room temperature the N,N-dimethylformamide was removed under reduced pressure and the resulting residue was partitioned between dichloromethane (60 mL) and water (60 mL). The organic phase was washed with water (60 mL), brine (60 mL), dried over magnesium sulfate, filtered and the solvent removed under reduced pressure to afford acetic acid 2-(2-ethoxy-naphthalen-1-yl)-2-oxo-ethyl ester (6.1 g, 94%) as dark red oil. 1H NMR (CDCl3): 1.45 (3H, t, J=7.0 Hz), 2.2 (3H, s), 4.2 (2H, q, J=7.0 Hz), 5.15 (2H, s), 7.2 (1H, d, J=9.4 Hz), 7.35 (1H, m), 7.45 (1H, m), 7.75 (1H, d, J=8.1 Hz), 7.85 (2H, m).

Workup

  1. customwas removed under reduced pressure
  2. customthe resulting residue was partitioned between dichloromethane (60 mL) and water (60 mL)
  3. washThe organic phase was washed with water (60 mL), brine (60 mL)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customthe solvent removed under reduced pressure

Sources & evidence

ORD record
ord-57ef121f30984db79b7ad37dc62c324e
Source dataset
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07429607B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes