戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1110882作成日:2026年10月25日

Ethyl Acetate → 5-Fluoro-1-(4-fluorophenyl)indoline-2,3-dione

https://huagongshe.com/reaction/1110882

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Oxalyl chlorideHCID 65578—
反応物Aluminum(III) ChlorideHCID 6451240—
反応物4-Fluoro-N-(4-fluorophenyl)benzenamineHCID 11241173—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物5-Fluoro-1-(4-fluorophenyl)indoline-2,3-dioneHCID 13339551—

反応手順

Oxalyl chloride (9.62 ml, 0.11 mole) was dissolved in 45 ml CH2Cl2. A solution of di-(4-fluorophenyl)amine (19.7 g, 0.096 mole) in 145 ml CH2Cl2 was added over 15 minutes; the temperature rose from 23° to 28°. After stirring 1 hour, AlCl3 (40.8 g) was added portionwise over 15 minutes; the temperature rose from 20° to 30°, and was kept less than 30° by cooling.. After stirring for 10 minutes, the reaction mixture was added to 250 ml ethyl acetate and 500 ml ice and water (the temperature rose to 30° C.). The aqueous layer was washed 2×250 ml ethyl acetate The organic layers were combined, back-washed 1×400 ml H2O, dried over MgSO4, evaporated to solids and triturated with 100 ml 1:1 ether:hexane to recover title product, 19.9 g, m.p. 180°-190°, tlc Rf 0.55 (1:1 ether;hexane)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04977178
出典データセットuspto-grants-1990_12
ORD IDord-30b3e43c48ad4b0ca8c824f0275bc5f1
出典メモuspto-grants-1990_12