反応 #1172

ord-554bd9dd465641989667d60605d8d5a8

反応方程式

OC1CCNCC1
4-Hydroxypiperidine
CCN(CC)CC
Et3N
O=C(Cl)OCc1ccccc1
benzyl chloroformate
CO.ClC(Cl)Cl
CHCl3 MeOH
O=C(OCc1ccccc1)N1CCCCC1
N-Cbz-piperidine
収率 59.2%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.ADDITIONwas added

実験手順

4-Hydroxypiperidine (10.8 g, 107 mmol) and Et3N (17 mL, 123 mmol) in 80 mL of CH2Cl2 was cooled in an ice bath whereupon benzyl chloroformate (16.3 mL, 114 mmol) was added. After stirring 1.5 h at R.T. the mixture was subjected to standard work-up conditions to give 13.9 g (55%) of N-Cbz-piperidine after chromatography (CHCl3 /MeOH; 10:1). [1H]-NMR(CDCl3) consistent with structure.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723490uspto-grants-1998_03