戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 261841作成日:2026年10月27日

Pyridine → alpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate

https://huagongshe.com/reaction/261841

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物2-(4-Chlorophenyl)-3-methylbutanoyl chlorideHCID 4178001—
反応物2,2,2-Trifluoro-1-(3-phenoxyphenyl)ethan-1-olHCID 14270571—
溶媒TolueneHCID 1140—
生成物alpha-Trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoateHCID 5381839098.3%

反応手順

This compound was prepared in the manner of Example II, using 5.3 g of 2-(4-chlorophenyl)-3-methylbutanoyl chloride, whose preparation is described in Agr. Biol. Chem., 38, 881 (1974), together with J. Kagaku To Seibutsu, 14, 427 (1976), 4.6 g of α-trifluoromethyl-3-phenoxybenzyl alcohol, and 1.5 g of pyridine in 50 ml of toluene. Volatiles were removed from the crude reaction product at 100° C./0.02 mm through a short path Kugelrohr distillation system to give as a residue 7.8 g of α-trifluoromethyl-3-phenoxybenzyl 2-(4-chlorophenyl)-3-methylbutanoate. The ir spectrum was consistent with the assigned structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152455
出典データセットuspto-grants-1979_05
ORD IDord-2168c1c5860e41bcbe412bf4e1bd93fc
出典メモuspto-grants-1979_05