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1245645-99-1

2,4-dicyclopropylbenzaldehyde synthesis

1synthesis methods
411235-57-9 Synthesis
Cyclopropylboronic acid

411235-57-9
435 suppliers
$6.00/1g

2,4-dicyclopropylbenzaldehyde

1245645-99-1
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Yield:1245645-99-1 68%

Reaction Conditions:

with potassium phosphate tribasic heptahydrate;C45H53ClFeNO2PPd in water;toluene at 100; for 5.5 h;Inert atmosphere;Suzuki coupling;

Steps:

4.2. General experimental procedure

General procedure: Potassium phosphate (0.75 mmol) and IIe (1 mol %) was added to the solution of aryl halides (0.25 mmol) and cyclopropylboronic acid (0.5 mmol) in toluene (2.0 mL) and water (100 μL). The mixture was heated to 100 °C for a proper time under nitrogen atmosphere and cooled to room temperature. Water (10 mL) was added and the mixture was extracted with EtOAc (3×15 mL), evaporated and purified by chromatography on silica gel.

References:

Zhang, Min;Cui, Xiuling;Chen, Xiaopei;Wang, Lianhui;Li, Jingya;Wu, Yusheng;Hou, Lifen;Wu, Yangjie [Tetrahedron,2012,vol. 68,# 3,p. 900 - 905] Location in patent:experimental part