(Diethylamino)sulfur trifluoride → 4-Allyl-4-fluoro-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester
Reaktionsgleichung
CCN(S(F)(F)[F:7])CC.[CH3:10][O:11][C:12]([CH:14]1[CH2:18][C:17]([CH2:20][CH:21]=[CH2:22])(O)[CH2:16][N:15]1[C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])=[O:13]>C(Cl)Cl>[CH3:10][O:11][C:12]([CH:14]1[CH2:18][C:17]([CH2:20][CH:21]=[CH2:22])([F:7])[CH2:16][N:15]1[C:23]([O:25][C:26]([CH3:29])([CH3:28])[CH3:27])=[O:24])=[O:13]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- -78 °C
Versuchsvorschrift
To a stirred solution of DAST (1.06 g, 6.58 mmol) in DCM (10 mL) at −78° C., 4-allyl-4-hydroxy-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (940 mg, 3.3 mmol) in dry DCM (10 mL) was added slowly. The mixture was then stirred at −78° C. for 1 h, then at −10° C. for an additional 1 h. DCM (50 mL) was added, quenched with NH4Cl (10%, 150 mL) and the organic layer was separated, dried over sodium sulfate and evaporated to dryness. The residue obtained on removal of solvent was purified by silica gel column chromatography using 5% EtOAc in hexanes as eluent to obtain 4-allyl-4-fluoro-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester (330 mg, 34%).
Aufarbeitung
- waitat −10° C. for an additional 1 h
- customquenched with NH4Cl (10%, 150 mL)
- customthe organic layer was separated
- dry with materialdried over sodium sulfate
- customevaporated to dryness
- customThe residue obtained on removal of solvent
- customwas purified by silica gel column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-cdeee53bce4c4a419b4c40143007810d
- Quelldatensatz
- uspto-grants-2007_04
- Patentnummer
- US07199105B2
Notizen zur Reaktion
Wird geladen…