4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)but-2-enoic acid ethyl ester → 4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)-butyric acid ethyl ester

HRID 1454082Notes

Reaction equation

HRID 1454082 reaction equation
[CH2:1]([O:3][C:4](=[O:16])[C:5]([CH2:11][C:12]([F:15])([F:14])[F:13])=[CH:6][C:7]([F:10])([F:9])[F:8])[CH3:2]>C1COCC1.[Pd]>[CH2:1]([O:3][C:4](=[O:16])[CH:5]([CH2:11][C:12]([F:13])([F:14])[F:15])[CH2:6][C:7]([F:8])([F:10])[F:9])[CH3:2]

Participants

4

Procedure

4,4,4-Trifluoro-2-(2,2,2-trifluoroethyl)-but-2-enoic acid ethyl ester (225 g, 0.9 mol) was dissolved in THF (700 mL) and treated with 5% Pd/C (17 g). The mixture was reduced by hydrogenation in a “Parr” shaker in a 2.5 L pressure bottle at 50 psi. The reaction was exothermic to 45° C. and was controlled by interrupting the shaking motion of the “Parr” shaker. The reaction was completed in approximately 2 hours. The reaction mixture was filtered through a 2-inch bed of the Solka Floc® reagent/magnesium sulfate to give a clear, colorless solution of the title compound (225 g in 1182 g of tetrahydrofuran, quantitative yield). Mass Spectrum (+ESI): 253 [M+H]+

Workup

  1. customwas exothermic to 45° C.
  2. filtrationThe reaction mixture was filtered through a 2-inch bed of the Solka Floc® reagent/magnesium sulfate

Sources & evidence

ORD record
ord-1c4ea47598c54864a6c209f668f1a091
Source dataset
uspto-grants-2009_01
Patent number
US07476762B2

Reaction notes

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