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HRID 972008作成日:2026年10月23日

Pyridine → alpha-Trifluoromethyl-3-phenoxybenzyl 3-(2,2-dimethylvinyl)-2,2-dimethylcyclopropanecarboxylate

https://huagongshe.com/ja/reaction/972008

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物(1R-trans)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropanecarbonyl chlorideHCID 26620—
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 3-(2,2-dimethylvinyl)-2,2-dimethylcyclopropanecarboxylateHCID 1285531593.9%

反応手順

This compound was prepared in the manner of Example II using 3.3 g of 2,2-dimethyl-3-(2-methyl-1-propenyl)cyclopropanecarbonyl chloride, whose preparation is described in J. Sci. Food and Agriculture, 18, 325 (1967), 4.3 g of α-trifluoromethyl-3-phenoxybenzyl alcohol, and 1.5 g of pyridine in 50 ml of toluene. Volatiles were distilled from the crude reaction product at 90°/0.08 mm for 1/2 hour, then at 100°/0.08 mm for 3/4 hour through a short path Kugelrohr distillation system to give as a residue 6.3 g of α-trifluoromethyl-3-phenoxybenzyl 3-(2,2-dimethylvinyl)-2,2-dimethylcyclopropanecarboxylate. 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US04162366
出典データセットuspto-grants-1979_07
ORD IDord-a7ee1ca9f5ec4af6a9783841f21d0c35
出典メモuspto-grants-1979_07