돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11317생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/11317

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Succinic anhydrideHCID 7922—
반응물Ethyl 2-(2-chlorophenoxy)acetateHCID 302826—
반응물Aluminum(III) ChlorideHCID 6451240—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매HexaneHCID 8058—
생성물4-[3-Chloro-4-(ethoxycarbonylmethoxy)phenyl]-4-oxobutyric acidHCID 1487828846%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098211B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-eae56509a51f4eea830b1991cad1252d
출처 메모uspto-grants-2006_08