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HRID 48320作成日:2026年10月24日

Chlorotrimethylsilane → Diethyl [2-(2-Fluorophenyl)-2-oxoethyl]phosphonate

https://huagongshe.com/ja/reaction/48320

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
反応物2-Fluorobenzoyl chlorideHCID 9808—
反応物(Diethoxyphosphinyl)acetic acidHCID 36704—
反応物Magnesium ChlorideHCID 5360315—
溶媒TolueneHCID 1140—
生成物Diethyl [2-(2-Fluorophenyl)-2-oxoethyl]phosphonateHCID 8658580864.4%

反応手順

To a solution of 2.34 g (11.9 mmol) of diethylphosphonoacetic acid in toluene at 0° C. was added 4.82 g (47.7 mmol) of triethylamine followed by 1.94 g (17.9 mmol) of chlorotrimethylsilane. The mixture was stirred at ambient temperature for 1 hour, then 1.13 g (11.9 mmol) of magnesium chloride was added and the mixture was stirred for a further 1 hour. To the mixture was added 2.0 g (14.3 mmol) of 2-fluorobenzoyl chloride and the mixture was stirred for 72 hours. The mixture was partitioned between 200 ml of water and 250 ml, 100 ml of dichloromethane. The combined organic portions were dried (magnesium sulphate), filtered and evaporated. The residue was purified by column chromatography eluting with 3-5% methanol/dichloromethane to give 2.1 g (64%) of [2-(2-fluorophenyl)-2-oxoethyl]phosphonic acid diethyl ester as a colorless oil; MS: m/e 274.9 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703387B2
出典データセットuspto-grants-2004_03
ORD IDord-b0e8ef5bf537437c815fb0e222c755ee
出典メモuspto-grants-2004_03