Hydrochloric Acid → HCID 19047214, compound

HRID 2210872Notes

Reaction equation

HRID 2210872 reaction equation
[F:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH:13]=[CH:14][C:15]([OH:17])=[O:16].Cl>CO.[Pd]>[F:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16]

Participants

5

Procedure

The methyl ester of 14-fluoro-2-tetradecenoic acid (3.3 g) was dissolved in methanol (20 ml), in which 10% palladium/carbon (0.9 g) was suspended, and a 10% methanolic hydrochloric acid solution (2 ml) was added. The mixture was stirred under hydrogen atmosphere for 12 hours. The reaction mixture was filtered, and a large amount of chloroform was added to the filtrate. The chloroform layer was washed with a saturated aqueous sodium hydrogen carbonate solution and water. The organic layer was dried and concentrated to give the methyl ester of 14-fluorotetradecanoic acid (2.5 g). The methyl ester (2.5 g) was dissolved in a solution of potassium hydroxide in ethanol-water (1:1), and the mixture was stirred at 80° C. for 30 minutes. The reaction mixture was acidified by adding citric acid and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated to give 14-fluorotetradecanoic acid (2.3 g).

Workup

  1. filtrationThe reaction mixture was filtered
  2. additiona large amount of chloroform was added to the filtrate
  3. washThe chloroform layer was washed with a saturated aqueous sodium hydrogen carbonate solution and water
  4. customThe organic layer was dried
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-574ed5a72b6b407d80116a77788199d1
Source dataset
uspto-grants-1995_10
Patent number
US05461036

Reaction notes

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