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HRID 485707作成日:2026年10月26日

Dicyclohexylcarbodiimide → 5-benzyl-3-furyl-methyl (1R,cis)2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate

https://huagongshe.com/reaction/485707

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物3-Furanmethanol, 5-(phenylmethyl)-HCID 12364396—
反応物(1R,3S)-2,2-Dimethyl-3-propadienylcyclopropane-1-carboxylic acidHCID 13309114—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物5-benzyl-3-furyl-methyl (1R,cis)2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylateHCID 5454193784.5%

反応条件

温度0 °C

反応手順

4.06 g of dicyclohexylcarbodiimide were added at 0° C. to a solution of 1.52 g of (1R,cis)2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane carboxylic acid in 40 ml of methylene chloride followed by addition of a few crystals of 4-dimethylaminopyridine and stirring at 0° C. for 15 minutes. A solution of 2.07 g of 5-benzyl-3-furyl-methanol in 10 ml of methylene chloride were added at 0° C. to the mixture which was stirred at 20° C. for 4 hours and was then filtered. The filtrate was evaporated to dryness under reduced pressure and the residue was chromatographed over silica gel. Elution with a 1-1 benzene-petroleum ether (b.p.=35° to 70° C.) yielded 2.72 g of 5-benzyl-3-furyl-methyl (1R,cis)2,2-dimethyl-3-(1,2-propadienyl)-cyclopropane-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04537897
出典データセットuspto-grants-1985_08
ORD IDord-304b9272d1af44d0abec985c17edaa23
出典メモuspto-grants-1985_08