反应 #1172

ord-554bd9dd465641989667d60605d8d5a8

反应方程式

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
收率 59.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.ADDITIONwas added

实验过程

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.

来源

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