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HRID 5950作成日:2026年10月24日

Lithium iodide → [2R,3R]-2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanone

https://huagongshe.com/ja/reaction/5950

反応式

関与物質

役割名称HCID仕込み量
反応物Lithium iodideHCID 66321—
反応物[4R,5R]-4,5-bis(((1,1-dimethylethyl)-dimethylsilyl)oxymethyl)-1-oxaspiro[2,2]pentaneHCID 18648066—
溶媒DichloromethaneHCID 6344—
生成物[2R,3R]-2,3-Bis(((1,1-dimethylethyl)dimethylsilyl)oxymethyl)cyclobutanoneHCID 54324527—

反応条件

温度0 °C

反応手順

A solution of 12.752 g (35.6 mmol) of [4R,5R]-4,5-bis(((1,1-dimethylethyl)-dimethylsilyl)oxymethyl)-1-oxaspiro[2,2]pentane, from Step D, in 50 mL of methylene chloride was added to a solution of 3.814 g (28.5 mmol) of lithium iodide in 200 mL of methylene chloride which had been cooled in an ice bath. After stirring the reaction mixture for 1 h at 0° C., the ice bath was removed and the reaction mixture was stirred for 20 minutes at ambient temperature. The reaction mixture was then washed with 5% aqueous sodium bicarbonate solution, 5% sodium bisulfite solution and brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure to give 12.317 g (96.6% crude yield) of the title compound which was taken on to the next step without purifiaction; MS DCI-NH3M/Z: 376 (M+NH4)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05246931
出典データセットuspto-grants-1993_09
ORD IDord-7ec30e53b2a04dcaad75f537b4457fc2
出典メモuspto-grants-1993_09