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HRID 1484作成日:2026年10月24日

Ethyl Acetate → 2-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dione

https://huagongshe.com/ja/reaction/1484

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物3,4,5,6-Tetrahydrophthalic anhydrideHCID 12475—
反応物4-Chloro-2-fluoroanilineHCID 93898—
反応物Water ethylacetateHCID 22728543—
溶媒Acetic AcidHCID 176—
生成物2-(4-Chloro-2-fluorophenyl)-4,5,6,7-tetrahydro-1h-isoindole-1,3(2h)-dioneHCID 18593169.3%

反応手順

A mixture of 4-chloro-2-fluoroaniline (19.0 g, 130.6 mmol), and 3,4,5,6-tetrahydrophthalic anhydride (19.85 g, 130.6 mmol) in acetic acid (150 mL) is refluxed for 2 hours, treated with additional 4-chloro-2-fluoroaniline (3.0 g), refluxed for 90 minutes, stirred at room temperature overnight and poured into a water/ethyl acetate mixture. The organic phase is washed sequentially with water, saturated sodium hydrogen carbonate solution and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to obtain a purple oil. Flash column chromatography of the oil using silica gel and 15% to 20% ethyl acetate in hexanes solutions gives the title product as an off-white solid (25.3 g, mp 81°-82° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726126
出典データセットuspto-grants-1998_03
ORD IDord-3ce2e94879794c84802f9843f2d4155a
出典メモuspto-grants-1998_03