Methyl iodide → benzyl (2S,4R)-2-(fluoromethyl)-4-methoxypyrrolidine-1-carboxylate

HRID 1852747Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1852747
[F:1][CH2:2][C@@H:3]1[CH2:7][C@@H:6]([OH:8])[CH2:5][N:4]1[C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10].[CH3:19]I.[H-].[Na+]>C1COCC1>[F:1][CH2:2][C@@H:3]1[CH2:7][C@@H:6]([O:8][CH3:19])[CH2:5][N:4]1[C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)=[O:10]

Komponenten

5

Versuchsvorschrift

To a solution of benzyl (2S,4R)-2-(fluoromethyl)-4-hydroxypyrrolidine-1-carboxylate (500 mg, 1.97 mmol) in THF (6.6 mL) at 0° C. was added methyl iodide (0.43 mL, 3.44 mmol) followed by sodium hydride (104 mg, 4.34 mmol). The mixture was stirred for 2 hours at room temperature. The reaction was quenched with ice, and diluted with diethyl ether. The organic layer was washed with water and brine, dried over sodium sulfate, filtered and concentrated under reduced pressure to afford benzyl (2S,4R)-2-(fluoromethyl)-4-methoxypyrrolidine-1-carboxylate. MS ESI calc'd. for C14H18FNO3 [M+H]+ 268. found 268.

Aufarbeitung

  1. customThe reaction was quenched with ice
  2. additiondiluted with diethyl ether
  3. washThe organic layer was washed with water and brine
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-b6cb102ee8294e3e973a21c595f538b5
Quelldatensatz
uspto-grants-2015_02
Patentnummer
US08962611B2

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