Reaktion #1764250

Reaktionsgleichung

tetrahydrofuran

(2R,5S)-5-(4-fluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester

Water

→

title compound

Ausbeute 100.0%

(2S,5R)-2-(4-fluorophenyl)-5-hydroxymethyl-pyrrolidine-1-carboxylic acid t-butyl ester

Ausbeute 100.0%

Lösungsmittel

ethyl acetate

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe organic layer was partitioned
2. 2
   WaschenThe organic layer was washed with brine
3. 3
   Trocknenthe resultant was dried over anhydrous magnesium sulfate
4. 4
   SonstigeThe solvent was removed under a vacuum

Vorschrift

Ice-cold lithium borohydride (256 mg) was added to a tetrahydrofuran (30 mL) solution of (2R,5S)-5-(4-fluorophenyl)pyrrolidine-1,2-dicarboxylic acid 1-t-butyl ester 2-ethyl ester (2.64 g) obtained in Example 4. Stirring was continued for 30 minutes at the same temperature and for 14 hours at room temperature. Water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine, and the resultant was dried over anhydrous magnesium sulfate. The solvent was removed under a vacuum, and the title compound (2.31 g) was obtained. The physical property values are as follows.

Quelle