反応 #69916

ord-ba1997f8267f41bdbd91c83964a90e0e

溶媒

反応条件

温度
0°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    洗浄washed with water (2×250 mL)
  2. 2
    乾燥The organic layer was dried over anhydrous Na2SO4
  3. 3
    ろ過filtered
  4. 4
    濃縮concentrated by rotary evaporation

実験手順

4-(3-Hydroxymethylfuran-2-yl)piperidine-1-carboxylic acid t-butyl ester (0.3 g, 1.1 mmol, 1.0 eq.) was dissolved in DCM (5.7 mL). The mixture was cooled to 0° C. and DABCO (132 mg, 1.2 mmol, 1.1 eq.) was added, followed by TsCl (224 mg, 1.2 mmol, 1.1 eq.). The mixture was stirred at 0° C. for 90 minutes, then diluted with EtOAc (500 mL) and washed with water (2×250 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated by rotary evaporation to yield the title compound (233 mg), which was used without further purification.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08530663B2uspto-grants-2013_09