首页> 外文期刊>Journal of Labelled Compounds and Radiopharmaceuticals >EVALUATION OF [~11C]FORMYL CHLORIDE AS A CARBON-11 FORMYLATION AGENT: SYNTHESIS OF iV-(4-TOLYL)-[~11C] ORMAMIDE AS A MODEL REACTION
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EVALUATION OF [~11C]FORMYL CHLORIDE AS A CARBON-11 FORMYLATION AGENT: SYNTHESIS OF iV-(4-TOLYL)-[~11C] ORMAMIDE AS A MODEL REACTION

机译:作为碳11甲酰化剂的[〜11C]甲酰氯的评估:作为模型反应的iV-(4-甲苯基)-[〜11C]甲酰胺的合成

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摘要

Formyl chloride was generated for the first time in 196.3 (1). This acid chloride of formic acid is stable below -60癈. At higher temperatures it dissociates spontaneously into carbon monoxide and hydrochloric acid. Recently, a new, highly efficient method for the preparation of formyl chloride at -78degC appeared in the literature (2): A complex made of hexachloroacetone (HCA) and two equivalents of triphenylphosphine (TPP) reacted at -78degC with formic acid to give formyl chloride, which was subsequently used in iV-formylation reactions.
机译:甲酰氯在196.3年首次产生(1)。该甲酸的酰氯在-60℃以下稳定。在较高的温度下,它会自发分解为一氧化碳和盐酸。最近,在文献(2)中出现了一种新的高效制备甲酰氯的方法(2):由六氯丙酮(HCA)和两当量的三苯膦(TPP)制成的络合物在-78℃与甲酸反应生成甲酰氯,其随后用于IV甲酰化反应。

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