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HRID 1864813作成日:2026年10月24日

Trimethylsilyldiazomethane → Methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoate

https://huagongshe.com/ja/reaction/1864813

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylsilyldiazomethaneHCID 167693—
反応物2-{[2-(3,5-Difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoic acidHCID 66973305—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物Methyl 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoateHCID 66973283—

反応手順

To a solution of 2-{[2-(3,5-difluorophenyl)-2-oxoethyl]thio}-2-methylpropanoic acid from Step A (400. mg, 1.46 mmol) in MeOH (3 mL), was added trimethylsilyldiazomethane (2 M in hexanes) until yellow color persists. The reaction mixture was stirred for an additional twenty minutes. The reaction mixture was diluted with ether (30 mL) and water (10 mL). The organics were washed with 5% sodium bicarbonate and then with saturated brine. The organics were dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue. This residue was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:Hexanes-40:60 to 90:10, to give the title compound. MS: m/z=229 (M−CO2Me).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07625901B2
出典データセットuspto-grants-2009_12
ORD IDord-69336b16ee384dd68d3fcc2f60ba1aee
出典メモuspto-grants-2009_12