反应 #45472

ord-45b276a754ff450c806d14b42c192eab

反应方程式

C#CC(OCC)OCC
3,3-diethoxy-1-propyne
CC1(C)OBOC1(C)C
4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CCN(CC)CC
Triethylamine
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
title compound
收率 53.0%
CCOC(/C=C/B1OC(C)(C)C(C)(C)O1)OCC
2-[(E)-3,3-diethoxy-1-propenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
收率 53.0%

反应条件

温度
50°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the solvent was removed in vacuo
  2. 2
    workup.DISTILLATIONThe residue was distilled at 90° C. at 10 torr
  3. 3
    其他The residue was purified by column chromatography on neutral alumina using 89:10:1 dichloromethane
  4. 4
    其他The solvent was removed in vacuo

实验过程

A mixture of 3,3-diethoxy-1-propyne (18.5 g, 0.144 mol), 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (27.6 g, 0.216 mol) and bis(cyclopentadienyl)zirconium chloride hydride (1.9 g, 0.007 mol) in tetrahydrofuran (75 mL) was heated at 50° C. for 2 days. Triethylamine (2 mL) was added and the solvent was removed in vacuo. The residue was distilled at 90° C. at 10 torr. The residue was purified by column chromatography on neutral alumina using 89:10:1 dichloromethane: ethyl acetate: triethylamine as an eluent. The solvent was removed in vacuo to give the title compound (15.9 g, 53%) as a brown oil. 1H NMR (DMSO-d6, 400 MHz) δ 6.48 (dd, 1H), 5.75 (d, 1H), 4.85 (d, 1H), 3.55-3.67 (m, 2H), 3.40-3.52 (m, 2H), 1.22 (s, 12H), 1.17 (t, 6H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07737160B2uspto-grants-2010_06