Sodium Hydroxide → HCID 11809522, compound
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]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- temperaturewhile cooling in an ice bath
- customethanol was evaporated under reduced pressure
- additionThe thus obtained residue was mixed with water (50 ml)
- washwashed with dichloromethane (50 ml×2)
- temperaturethe thus separated aqueous layer was cooled in an ice bath
- additionby adding dropwise concentrated hydrochloric acid
- extractionextracted with diethyl ether (100 ml×5)
- customsubsequently drying the
- extractionextract over anhydrous magnesium sulfate
- filtrationAfter filtration
- concentrationthe filtrate was concentrated under reduced pressure
- dissolutionthe thus obtained residue was dissolved in benzene (100 ml)
- 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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