反应 #1328393

ord-19973adf1ffc4b7a90c600a2c7712cbe

反应方程式

O=C(Cl)OCc1ccccc1
benzyl chloroformate
NCCCO
3-aminopropanol
O=C(NCCCO)OCc1ccccc1
title compound
收率 58.9%
O=C(NCCCO)OCc1ccccc1
N-CBZ-3-aminopropanol
收率 58.9%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤The reaction mixture was washed with H2O
  2. 2
    其他dried
  3. 3
    其他purified by flash column chromatography (on silica gel, CH3OH—CH2Cl2)

实验过程

A CH2Cl2 solution (300 mL) of 3-aminopropanol (10 g, 0.133 mole) and TEA (20 g, 0.2 mole) was cooled to 0° C., followed by slow addition of CH2Cl2 solution (25 mL) of benzyl chloroformate (25 g, 0.147 mole). The resulting solution was gradually warmed to room temperature. The stirring was continued at room temperature overnight. The reaction mixture was washed with H2O, dried and purified by flash column chromatography (on silica gel, CH3OH—CH2Cl2) to yield 16.4 g, 58.9% of title compound. 1H NMR (CDCl3): δ 7.26-7.40 (m, 5H), 5.10 & 5.0-5.10 (s+m, 3H), 3.68 (q, 2H), 3.36 (q, 2H), 2.58 (t, 1H), 1.70 (p, 2H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE039324E1uspto-grants-2006_10