Beta-Propiolactone → HCID 64853602, compound

HRID 1774582Notes

Reaction equation

HRID 1774582 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[OH:9].CC(C)([O-])C.[K+].[C:16]1(=[O:20])[O:19][CH2:18][CH2:17]1>O1CCCC1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][C:3]=1[O:9][CH2:18][CH2:17][C:16]([OH:20])=[O:19]

Participants

5

Procedure

To a suspension of 2-fluoro-5-methylphenol (1.0 g, 7.9 mmol) in tetrahydrofuran (10 mL) at 0-5° C. was dropwise added potassium tert-butoxide 1N in tetrahydrofuran (8.3 mL, 8.3 mmol), followed by 3-propiolactone (0.55 mL, 8.7 mmol) in one portion. The mixture was warmed to room temperature for 1 hour, then heated at 50° C. for 2 hours. After cooling to room temperature, the mixture was quenched with a saturated solution of sodium hydrogenocarbonate (1 mL) and diluted with water (9 mL). The aqueous layer was washed with ethyl acetate (10 mL), acidified with 1M hydrochloric acid until pH 2 and extracted with ethyl acetate (2×10 mL). The organic layer was dried over sodium sulfate and concentrated in vacuo to provide 3-(2-fluoro-5-methylphenoxy)propanoic acid (10a) (0.96 g, 4.8 mol, 60%) which was used without further purification.

Workup

  1. temperatureheated at 50° C. for 2 hours
  2. temperatureAfter cooling to room temperature
  3. customthe mixture was quenched with a saturated solution of sodium hydrogenocarbonate (1 mL)
  4. additiondiluted with water (9 mL)
  5. washThe aqueous layer was washed with ethyl acetate (10 mL)
  6. extractionextracted with ethyl acetate (2×10 mL)
  7. dry with materialThe organic layer was dried over sodium sulfate
  8. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-d567f6f9c11140089bb79aefab64f28e
Source dataset
uspto-grants-2016_02
Patent number
US09260395B2

Reaction notes

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