反应 #543591

ord-5075cc30b00d4274928acde9ee30045f

反应方程式

OCc1ccc(N2CCN(Cc3ccccc3)CC2)cc1
[4-(4-Benzyl-piperazin-1-yl)phenyl]-methanol
OCc1ccc(N2CCNCC2)cc1
title compound
收率 100.0%
OCc1ccc(N2CCNCC2)cc1
(4-Piperazin-1-yl-phenyl)-methanol
收率 100.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Hydrogen was bubbled through the suspension for 1 h
  2. 2
    过滤The catalyst was filtered off
  3. 3
    其他the solvent removed in vacuo

实验过程

To a solution of [4-(4-Benzyl-piperazin-1-yl)phenyl]-methanol in EtOH (50 ml) under a blanket of argon was added a suspension of 10% palladium on charcoal (1.5 g) in EtOH (150 ml). Hydrogen was bubbled through the suspension for 1 h and then the reaction mixture was stirred under a blanket of hydrogen for 60 h at RT. The catalyst was filtered off and the solvent removed in vacuo to yield the title compound as a white solid (4.8 g, 100%). 1H-NMR δ (CDCl3) 7.30–7.21 (2H, m, ArH), 6.94–6.88 (2H, m, ArH), 4.59 (2H, s), 3.18–2.98 (8H, m). HPLC: 0.5 min (37%@214 nm), 0.7 min (55%@214 nm), multiple peaks due to salt formation from TFA buffer; LRMS +ve: 193 (M+1, 70).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07186719B2uspto-grants-2007_03