Sodium Thiosulfate → (R)-2-Methyl-4,4,4-trifluorobutanal

HRID 2266871Notes

Reaction equation

HRID 2266871 reaction equation
[F:1][C:2]([F:9])([F:8])[CH2:3][C@@H:4]([CH3:7])[CH2:5][OH:6].CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O.[O-]S([O-])(=S)=O.[Na+].[Na+]>C(Cl)Cl.C(OCC)C.C([O-])(O)=O.[Na+]>[F:1][C:2]([F:9])([F:8])[CH2:3][C@@H:4]([CH3:7])[CH:5]=[O:6]

Participants

7

Conditions

Temperature
25 °C

Procedure

To (2R)-4,4,4-trifluoro-2-methylbutan-1-ol (2.90 g, 20.4 mmol) in CH2Cl2 (50 mL) at 0° C. was added Dess-Martin periodinane (10.24 g, 24.49 mmol). After 15 min, the reaction mixture was warmed to 25° C. and stirred for 1 h. This mixture was then diluted with diethyl ether (50 mL) and added to Na2S2O3 (11.29 g, 71.44 mmol) dissolved in a saturated solution of aqueous NaHCO3 (100 mL). The milky white mixture was stirred until both layers were homogeneous. The phases were separated and the organic extract was dried (MgSO4) and filtered to give a solution of (2R)-4,4,4-trifluoro-2-methylbutanal which was used in the next step without removal of solvents.

Workup

  1. stirringThe milky white mixture was stirred until both layers
  2. customThe phases were separated
  3. extractionthe organic extract
  4. dry with materialwas dried (MgSO4)
  5. filtrationfiltered

Sources & evidence

ORD record
ord-31a32c71561b469d838cb36ee4c9eec2
Source dataset
uspto-grants-2010_12
Patent number
US07858658B2

Reaction notes

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