Ammonium Chloride → 3-(2,4,6-Trifluoro-phenyl)-acrylic acid ethyl ester

HRID 474577

Reaction equation

HRID 474577 reaction equation
[CH2:1]([O:3][C:4](=[O:12])[CH2:5]P(OC)(OC)=O)[CH3:2].CC([O-])(C)C.[K+].[F:19][C:20]1[CH:27]=[C:26]([F:28])[CH:25]=[C:24]([F:29])[C:21]=1[CH:22]=O.[Cl-].[NH4+]>C1COCC1.CN(C=O)C.C1COCC1>[F:19][C:20]1[CH:27]=[C:26]([F:28])[CH:25]=[C:24]([F:29])[C:21]=1/[CH:22]=[CH:5]/[C:4]([O:3][CH2:1][CH3:2])=[O:12]

Participants

7

Procedure

To the solution of ethyl[bis(methyloxy)phosphoryl]acetate (1.980 mL, 11.99 mmol) in THF-DMF (60 mL, v/v=5:1) at 0° C. was added t-BuOK (1.458 g, 12.99 mmol) portion wise. The resultant mixture was stirred at room temperature for 30 minutes, then mixed with a solution of 2,4,6-trifluorobenzaldehyde (1.6 g, 9.99 mmol) in THF (10 mL) at 0° C. It was allowed to warm to room temperature and the mixture was stirred for 45 min. It was mixed with aqueous ammonium chloride and then extracted with ethyl acetate. The organic layer was washed with brine, dried over Na2SO4, filtered, and concentrated. The residue was purified by a flash column chromatography to give the title compound as a pale yellow oil (2.0 g, 87% yield). LCMS: rt=3.52 min, [M+H+]=231.1

Workup

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was washed with brine
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was purified by a flash column chromatography

Sources & evidence

ORD record
ord-e0957e9540054c5f81479c9091b0c6c2
Source dataset
uspto-grants-2014_01
Patent number
US08637536B2

Linked notes

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