反应 #1563913

ord-778f6346097a4e539f1db3a92bf75daf

反应方程式

O=Cc1ccc2c(c1)OCO2
piperonal
CC(C)(C)[O-].[K+]
t-BuOK
C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[I-]
methyltriphenylphosphonium iodide
C=Cc1ccc2c(c1)OCO2
5-vinylbenzo[d][1,3]dioxole
收率 94.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    workup.STIRRINGthe mixture was stirred for 1 h at 0° C
  2. 2
    浓缩The reaction mixture was concentrated
  3. 3
    其他the residue was purified by column chromatograph (petroleum ether)

实验过程

t-BuOK (7.77 g, 69.3 mmol) was added portions to a suspension of compound methyltriphenylphosphonium iodide (28.0 g, 68.3 mmol) in dry THF (250 mL) over 10 min at 0° C. The resulting yellow suspension was stirred for 20 min at this temperature. A solution of piperonal (8.0 g, 53.3 mmol) in dry THF (25 mL) was added dropwise to the above suspension and the mixture was stirred for 1 h at 0° C. The reaction mixture was concentrated and the residue was purified by column chromatograph (petroleum ether) to provide compound 5-vinylbenzo[d][1,3]dioxole (7.4 g, 94%) as colorless liquid. 1H-NMR (DMSO-d6): δ 5.09 (d, 1H, J=11.2 Hz), 5.68 (d, 1H, J=18 Hz), 6.00 (s, 2H), 6.63 (1, 1H, J1=11.2 Hz, J2=18 Hz), 6.85 (m, 2H), 7.11 (s, 1H).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09402832B2uspto-grants-2016_08