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HRID 2427423作成日:2026年10月25日

4-Methyl-2,3,5,6-tetrafluorobenzyl alcohol → 4-methyl-2,3,5,6-tetrafluorobenzyl (1R)-trans-3-(2-cyano-1-propenyl)-2,2-dimethylcyclopropanecarboxylate

https://huagongshe.com/reaction/2427423

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methyl-2,3,5,6-tetrafluorobenzyl alcoholHCID 2734209—
反応物(1R)-trans-3-(2-cyano-1-propenyl)-2,2-dimethylcyclopropanecarboxylic acidHCID 66664531—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-methyl-2,3,5,6-tetrafluorobenzyl (1R)-trans-3-(2-cyano-1-propenyl)-2,2-dimethylcyclopropanecarboxylateHCID 8665207871.5%

反応手順

Under a nitrogen atmosphere, 0.59 g of N,N-dicyclohexyl carbodiimide was added to a mixture of 0.55 g of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol, 0.51 g of (1R)-trans-3-(2-cyano-1-propenyl)-2,2-dimethylcyclopropanecarboxylic acid, 0.10 g of 4-dimethylaminopyridine and 7 ml of anhydrous dichloromethane, and the mixture was stirred at room temperature for 3 hours. Thereafter, the reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 0.72 g of 4-methyl-2,3,5,6-tetrafluorobenzyl(1R)-trans-3-(2-cyano-1-propenyl)-2,2-dimethylcyclopropanecarboxylate represented by the following formula:

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07968598B2
出典データセットuspto-grants-2011_06
ORD IDord-9d83daf7b22e4a7bac06476b8d8add05
出典メモuspto-grants-2011_06