Sulfuric Acid → (2R)-5,5,5-Trifluoro-2-hydroxypentanoic acid

HRID 2276858Notes

Reaction equation

HRID 2276858 reaction equation
N[C@H:2]([CH2:6][CH2:7][C:8]([F:11])([F:10])[F:9])[C:3]([OH:5])=[O:4].[OH:12]S(O)(=O)=O.N([O-])=O.[Na+]>O.CCOCC>[F:9][C:8]([F:11])([F:10])[CH2:7][CH2:6][C@@H:2]([OH:12])[C:3]([OH:5])=[O:4]

Participants

6

Conditions

Temperature
0 °C

Procedure

To a cool (0° C.), stirred solution of (2R)-2-amino-5,5,5-trifluoropentanoic acid (4.09 g, 23.90 mmol) (U.S. Publication No. 2009/0111858 A1) and H2SO4 (2.8 mL, 52.5 mmol) in water (95 mL) was added a solution of sodium nitrite (9.89 g, 143 mmol) in water (30 mL) dropwise via addition funnel over 60 min. The reaction mixture was allowed to slowly warm to room temperature and stirred overnight. The reaction mixture was diluted with Et2O, the aqueous phase was separated and extracted with Et2O (3×). The combined organics were dried (Na2SO4), filtered and concentrated under reduced pressure to provide Preparation 4B (4.1551 g, >99%) as an amber oil. 1H NMR (400 MHz, CDCl3) δ 4.33 (1H, dd, J=8.03, 4.27 Hz), 2.09-2.42 (3H, m), 1.88-2.02 (1H, m).

Workup

  1. additiondropwise via addition funnel over 60 min
  2. temperatureto slowly warm to room temperature
  3. customthe aqueous phase was separated
  4. extractionextracted with Et2O (3×)
  5. dry with materialThe combined organics were dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customto provide

Sources & evidence

ORD record
ord-4b90705e97924677bba4a934943dd602
Source dataset
uspto-grants-2015_09
Patent number
US09133139B2

Reaction notes

Loading…