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HRID 1920572作成日:2026年10月27日

Lithium Chloride → Ethyl (1-vinylcyclopropyl)acetate

https://huagongshe.com/reaction/1920572

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium ChlorideHCID 433294—
反応物Ethyl cyclopropylideneacetateHCID 11040705—
反応物HCID 178461836HCID 178461836—
触媒Cuprous chlorideHCID 62652—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl (1-vinylcyclopropyl)acetateHCID 57965754—

反応条件

温度-78 °C

反応手順

Under argon, 0.55 g (5.53 mmol) of copper(I) chloride and 0.59 g (13.82 mmol) of lithium chloride are suspended in 150 ml of anhydrous THF. The reaction mixture is cooled to −78° C., 48.8 ml (82.95 mmol) of vinylmagnesium chloride solution (1.7 M in THF) are added and the mixture is stirred for 10 minutes. Over a period of 30 min, a solution of 8.72 g (69.12 mmol) of ethyl cyclopropylideneacetate (Example 1A) in 50 ml of anhydrous THF is then added dropwise. After the addition is ended, the cooling bath is replaced by an ice/acetone bath. After a further 15 min, the reaction is terminated by dropwise addition of 100 ml of 1 N hydrochloric acid. The reaction mixture is saturated with sodium chloride, and 100 ml of a saturated sodium chloride solution which contains 5 ml of a 25% strength aqueous ammonia solution are then added. The mixture is filtered through Celite. The filtrate is washed with ammoniacal sodium chloride solution until the aqueous phase remains colorless. The organic phase is washed with saturated sodium chloride solution and dried over anhydrous magnesium sulfate. Removal of the solvent and kugelrohr distillation of the residue at 150° C. and 15 mbar gives 7.10 g (67% of theory) of the title compound as a colorless liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08168821B2
出典データセットuspto-grants-2012_05
ORD IDord-936a9b1f9b304f80b2d3cb84f193b2f6
出典メモuspto-grants-2012_05