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Geranilorcinol acetylated Derivatives of compounds. Synthesis procedure for obtaining these compounds and use of these compounds as antifungals against Botrytis cinerea

机译:Geranilorcinol乙酰化化合物的衍生物。获得这些化合物的合成方法以及这些化合物作为抗灰葡萄孢的抗真菌剂的用途

摘要

Refers to a synthesis procedure for linear geranilorcinoles acetylated Derivatives of compounds, comprising: preparing a Solution mixing Orcinol (1.22 G, 9.8 mmol), geraniol (1.51 G, 98 mmol) and acetonitrile (2ml); add the previous solution in a saturated solution of acetonitrile in AgNO3 (2ml); stir the solution at room temperature under nitrogen atmosphere; Inject slowly and directly bf3et2o (0.46 G, 32 mmol); stirring for 48 hours; add Crushed Ice (approximately 30 g) and abundant salt (NaCl); Vacuum filter; extracting the Organic Phase with acoet (3 x 20 ml); washing The Organic Phase with NaHCO3 Solution (15 ml, 5%) and Water (2 x 15 ml Dry over anhydrous Na2SO4), and Evaporated to filter and Dryness. It also refers to a compound of Formula 2 and 4.This Compound is useful as Antifungal against Botrytis cinerea
机译:指化合物的线性香叶菊酰乙酰化衍生物的合成方法,包括:制备混合了Orcinol(1.22 G,9.8 mmol),geraniol(1.51 G,98 mmol)和乙腈(2ml)的溶液;将先前的溶液加入乙腈在AgNO3(2ml)中的饱和溶液中;在室温下在氮气氛下搅拌溶液;缓慢直接注入bf3et2o(0.46 G,32 mmol);搅拌48小时;加入碎冰(约30 g)和大量盐(NaCl);真空过滤器;用牛油提取有机相(3 x 20 ml);用NaHCO 3溶液(15 ml,5%)和水(2 x 15 ml在无水Na 2 SO 4上干燥)洗涤有机相,并蒸发以过滤并干燥。它还指式2和4的化合物。该化合物用作抗灰葡萄孢的抗真菌剂。

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