HCID 90054371, compound → (R)-3,3-difluoro-5-(hydroxymethyl)pyrrolidin-2-one
Reaction equation
[F:1][C:2]1([F:13])[C:11](=[O:12])[N:5]2C(C)(C)[O:7][CH2:8][C@H:4]2[CH2:3]1>O.O1CCOCC1>[F:1][C:2]1([F:13])[CH2:3][C@H:4]([CH2:8][OH:7])[NH:5][C:11]1=[O:12]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 115 °C
Procedure
To a solution consisting of (R)-6,6-difluoro-3,3-dimethyltetrahydropyrrolo[1,2-c]oxazol-5(3H)-one (intermediate 6, 12.5 g, 65.4 mmol) in water-1,4-dioxane (300 mL, 1:1 v/v) was added Amberlite IR-120H*(6.23 g). The reaction mixture was heated to 115° C. for 6 hours and was subsequently filtered through Celite and washed with methanol. The filtrate was concentrated under reduced pressure, using toluene and ethanol additives to help drive off water, to provide a residue. The residue was washed with diethyl ether to afford the title compound as a tan solid (8.8 g; 89%), which was carried on without further purification; TLC Rf 0.25 (solvent system: 70:30 v/v ethyl acetate:hexanes). *Amberlite IR-120H ion-exchange resin, strongly acid gel-type resin with sulfonic acid functionality, CAS: 39389-20-3.75 g of Amberlite was washed and decanted three times with deionized water. The fourth wash was filtered using suction filtration and the semi-dry resin was quickly washed with 2-propanol then diethyl ether. The resin was dried to give 54 g of free flowing dark brown bead resin.
Workup
- additionwas added Amberlite IR-120H*(6.23 g)
- filtrationwas subsequently filtered through Celite
- washwashed with methanol
- concentrationThe filtrate was concentrated under reduced pressure
- customto provide a residue
- washThe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-9a35052d06954aae89787871c152aafb
- Source dataset
- uspto-grants-2015_11
- Patent number
- US09180116B2
Reaction notes
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