반응 #69916

ord-ba1997f8267f41bdbd91c83964a90e0e

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with water (2×250 mL)
  2. 2
    건조The organic layer was dried over anhydrous Na2SO4
  3. 3
    여과filtered
  4. 4
    농축concentrated by rotary evaporation

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08530663B2uspto-grants-2013_09