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Ethyl Acrylate → 2-((E)-2-Ethoxycarbonylvinyl)-4-trifluoromethylbenzoic Acid

HRID 2061635
Notes
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Reaction equation

HRID 2061635 reaction equation
N([O-])=O.[Na+].N[C:6]1[CH:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9].[H+].[B-](F)(F)(F)F.[C:25]([O:29][CH2:30][CH3:31])(=[O:28])[CH:26]=[CH2:27]>O.C(O)C>[CH2:30]([O:29][C:25](/[CH:26]=[CH:27]/[C:6]1[CH:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:12]=[CH:11][C:7]=1[C:8]([OH:10])=[O:9])=[O:28])[CH3:31]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 8821Ethyl AcrylateHCID 28118Tetrafluoroboric acid2×HCID 678694-(Trifluoromethyl)anthranilic acidHCID 23668193Sodium Nitrite

Product 1

HCID 576789502-((E)-2-Ethoxycarbonylvinyl)-4-trifluoromethylbenzoic Acid

Reagents, catalysts & solvents 2

HCID 702
Ethanol
Solvent
2×
HCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

520 mg of NaNO2 (7.6 mmol) were dissolved in 2 ml of water and added dropwise at 0° C. to a solution of 1.3 g of 2-amino-4-trifluoromethylbenzoic acid (6.5 mmol) in 2.6 ml of a 48% aqueous HBF4 solution and 30 ml of ethanol. The mixture was then stirred at 0° C. for 10 minutes, then warmed to RT. A further 0.3 ml of a 48% aqueous HBF4 solution was then added, then 30 ml of ethanol, 0.9 g of ethyl acrylate (9.0 mmol) and 26.9 mg of Pd (OAc)2 (0.12 mmol). Subsequently, the mixture was stirred at 50-60° C. for 1 h. The solvent was then removed under reduced pressure, and the residue taken up with 25 ml of EA and washed initially with 25 ml of a 1N aqueous HCl solution then with 25 ml of a saturated aqueous NaCl solution. The organic phase was dried over Na2SO4 and the solvent removed under reduced pressure. The residue was suspended in 25 ml of heptane and the precipitated product was filtered off. Yield: 1.3 g (69%) of a pale brownish solid. An analytical sample was purified by crystallization from heptane/ethyl acetate.

Workup

  1. temperaturewarmed to RT
  2. stirringSubsequently, the mixture was stirred at 50-60° C. for 1 h
  3. customThe solvent was then removed under reduced pressure
  4. washwashed initially with 25 ml of a 1N aqueous HCl solution
  5. dry with materialThe organic phase was dried over Na2SO4
  6. customthe solvent removed under reduced pressure
  7. filtrationthe precipitated product was filtered off
  8. customAn analytical sample was purified by crystallization from heptane/ethyl acetate

Sources & evidence

ORD record
ord-693509d8ef474c569a575536e44702e4
Source dataset
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08283374B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes