Water → HCID 178520944, compound

HRID 1515111Notes

Reaction equation

HRID 1515111 reaction equation
[F:1][C:2]([F:13])([F:12])[C@@H:3]1[CH2:8][CH2:7][C@H:6]([C:9](O)=[O:10])[CH2:5][CH2:4]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.[OH-].[Na+]>O1CCCC1>[F:1][C:2]([F:12])([F:13])[C@@H:3]1[CH2:4][CH2:5][C@H:6]([CH2:9][OH:10])[CH2:7][CH2:8]1

Participants

6

Conditions

Temperature
0 °C

Procedure

cis-4-(Trifluoromethyl)cyclohexanecarboxylic acid (1.5 g, 7.65 mmol) was dissolved in tetrahydrofuran (20 mL). The reaction solution was cooled to 0° C., and lithium aluminum hydride (435 mg, 11.5 mmol) was added thereto, and then, the resulting mixture was stirred at room temperature for 3 hours. The reaction solution was cooled to 0° C., and water (0.4 mL), a 5 N aqueous solution of sodium hydroxide (0.4 mL), and water (1.2 mL) were added thereto, followed by filtration. To the filtrate, ethyl acetate was added, and the organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and a saturated sodium chloride solution, then dried over anhydrous magnesium sulfate and filtered. Then, the solvent was distilled off under reduced pressure, whereby a crude product was obtained as a colorless oily substance (1.26 g).

Workup

  1. temperatureThe reaction solution was cooled to 0° C.
  2. filtrationfollowed by filtration
  3. additionTo the filtrate, ethyl acetate was added
  4. washthe organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate
  5. dry with materiala saturated sodium chloride solution, then dried over anhydrous magnesium sulfate
  6. filtrationfiltered
  7. distillationThen, the solvent was distilled off under reduced pressure, whereby a crude product
  8. customwas obtained as a colorless oily substance (1.26 g)

Sources & evidence

ORD record
ord-b3394a38bcda41359cf88342100bc2dd
Source dataset
uspto-grants-2012_07
Patent number
US08222281B2

Reaction notes

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