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HRID 42549作成日:2026年10月23日

Methanol → 2-Phenylpropan-2-yl 2,2,2-trichloroacetimidate

https://huagongshe.com/ja/reaction/42549

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TrichloroacetonitrileHCID 11011—
反応物2-Phenyl-2-propanolHCID 12053—
反応物Sodium hydrideHCID 24758—
溶媒Diethyl EtherHCID 3283—
生成物2-Phenylpropan-2-yl 2,2,2-trichloroacetimidateHCID 11140517103.7%

反応条件

温度0 °C

反応手順

A suspension of 60% sodium hydride in mineral oil (0.42 g, 10.50 mmol) in diethyl ether (10 mL) was treated with the dropwise addition of a solution of 2-phenylpropan-2-ol (12.02 mL, 86 mmol) in diethyl ether (30 mL). Upon completion of addition, the mixture was stirred for 30 minutes, during which time a nearly clear solution was observed. After this time, the mixture was cooled to 0° C. and then treated with the dropwise addition of trichloroacetonitrile (8.18 mL, 82 mmol), which caused the mixture to turn dark brown. The reaction was allowed to warm to room temperature over 1 hour, and then was concentrated in vacuo to yield a residue. The residue was dissolved in hexanes (10 mL) and treated with methanol (0.424 mL, 10.48 mmol), and the resulting mixture was stirred vigorously for 5 minutes. The resulting black suspension was filtered through glass fiberglass filter paper, and the collected solids were rinsed 3× with hexanes. The combined filtrates were concentrated in vacuo to yield 2-phenylpropan-2-yl 2,2,2-trichloroacetimidate (23.8 g, 85 mmol, 99% yield) as an amber oil which was used as-is in the next step.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536198B2
出典データセットuspto-grants-2013_09
ORD IDord-952eaeed0fab4cfeac741d18db575c11
出典メモuspto-grants-2013_09