Sodium Hydroxide → HCID 11809522, compound

HRID 1954607Notes

Reaction equation

HRID 1954607 reaction equation
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][C@@H:14]([C:16]2([C:19]([O:21]CC)=[O:20])[CH2:18][CH2:17]2)[C:13]([F:25])([F:24])[CH2:12]1)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>C(O)C>[CH2:1]([O:8][C:9]([N:11]1[CH2:12][C:13]([F:24])([F:25])[C@@H:14]([C:16]2([C:19]([OH:21])=[O:20])[CH2:18][CH2:17]2)[CH2:15]1)=[O:10])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Procedure

1-Benzyloxycarbonyl-4-(R)-(1-ethoxycarbonylcyclopropyl)-3,3-difluoropyrrolidine (2.287 g, 6.472 mmol) was dissolved in ethanol (65 ml) to which, while cooling in an ice bath, was added dropwise a 10 N sodium hydroxide aqueous solution (6.5 ml). The reaction solution was stirred at room temperature for 16 hours and then ethanol was evaporated under reduced pressure. The thus obtained residue was mixed with water (50 ml) and washed with dichloromethane (50 ml×2), and the thus separated aqueous layer was cooled in an ice bath, acidified by adding dropwise concentrated hydrochloric acid and then extracted with diethyl ether (100 ml×5), subsequently drying the extract over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure, and the thus obtained residue was dissolved in benzene (100 ml) and again concentrated under reduced pressure. This azeotropic treatment with benzene was repeated 3 times to obtain 1.956 g (92.9%) of the title compound as a colorless oil.

Workup

  1. temperaturewhile cooling in an ice bath
  2. customethanol was evaporated under reduced pressure
  3. additionThe thus obtained residue was mixed with water (50 ml)
  4. washwashed with dichloromethane (50 ml×2)
  5. temperaturethe thus separated aqueous layer was cooled in an ice bath
  6. additionby adding dropwise concentrated hydrochloric acid
  7. extractionextracted with diethyl ether (100 ml×5)
  8. customsubsequently drying the
  9. extractionextract over anhydrous magnesium sulfate
  10. filtrationAfter filtration
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. dissolutionthe thus obtained residue was dissolved in benzene (100 ml)
  13. concentrationagain concentrated under reduced pressure

Sources & evidence

ORD record
ord-803d2f1be000419fa19283ea6eb5f719
Source dataset
uspto-grants-2000_09
Patent number
US06121285

Reaction notes

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