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HRID 11317作成日:2026年10月25日

Hydrochloric Acid → 4-[3-Chloro-4-(ethoxycarbonylmethoxy)phenyl]-4-oxobutyric acid

https://huagongshe.com/reaction/11317

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Succinic anhydrideHCID 7922—
反応物Ethyl 2-(2-chlorophenoxy)acetateHCID 302826—
反応物Aluminum(III) ChlorideHCID 6451240—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒HexaneHCID 8058—
生成物4-[3-Chloro-4-(ethoxycarbonylmethoxy)phenyl]-4-oxobutyric acidHCID 1487828846%

反応手順

To a stirred solution of ethyl 2-chlorophenoxyacetate (32.0 g, 149 mmol) in dichloromethane (75 mL) at ambient temperature under nitrogen was added succinic anhydride (22.4 g, 224 mmol). The reaction mixture was cooled in ice-water and to this was added portion wise aluminum trichloride (59.6 g, 447 mmol), whilst maintaining the temperature below 20° C. The reaction mixture was then allowed to stir at ambient temperature for 20 minutes and was then heated to reflux and stirred at this temperature for 3 hours. The reaction mixture was allowed to cool to ambient temperature, then poured into a mixture of ice, water (200 ml) and HCl (10 N, 100 ml). The two phase system was separated and the aqueous layer was extracted with ethyl acetate (5×100 mL). All organic layers were then combined and washed with water (2×100 mL), dried over Na2SO4, and concentrated under reduced pressure to give an orange oily solid. Hexane (300 mL) was added, and after standing at ambient temperature for 1 hour, the precipitate was filtered off and re-crystallized from ethyl acetate/hexane to give 9 as a light yellow powder (21.5 g, 46% yield, 98% pure by LCMS and 1H NMR), 1H NMR (400 MHz; CDCl3): δ 7.79 (m, 1H); 7.66 (m, 1H); 6.79 (m, 1H); 4.90 (s, 2H); 4.12 (q, 2H); 2.82 (m, 2H); 2.42 (m, 2H); 1.30 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098211B2
出典データセットuspto-grants-2006_08
ORD IDord-eae56509a51f4eea830b1991cad1252d
出典メモuspto-grants-2006_08