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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2165080생성일: 2026년 10월 26일

Ethyl Acetate → HCID 12564414, 화합물

https://huagongshe.com/reaction/2165080

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Methanesulfonyl chlorideHCID 31297—
반응물Ethyl 5-chlorobenzofuran-2-carboxylateHCID 2799299—
반응물Aluminium lithium hydrideHCID 21226445—
용매PyridineHCID 1049—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물HCID 12564414HCID 1256441453.2%

반응 단계

To a suspension of ethyl-5-chloro-benzofuran carboxylate (1.05 g), prepared according to Helv. Chim. Acta., 818 (1935), in tetrahydrofuran (10 ml) was added lithium aluminum hydride (0.1 g). The mixture was stirred at room temperature for 1 hour. Ethyl acetate (50 ml) was slowly added to the reaction mixture, and the whole mixture was poured onto water (50 ml). The organic extract was separated, washed with water (2×25 ml), dried and evaporated to obtain 2-hydroxymethyl-5-cnlorobenzofuran as an oil [0.87 g; 'HNMR (CDCl3, 60 MHz): 4.6 (s, 2H), 6.6-7.4 (m, 4H)]. This material was added to a solution of methanesulfonyl chloride (1.15 g) in methylene chloride (20 ml) containing pyridine (1 ml). After stirring the reaction overnight it was poured onto ice-water (20 ml) and the organic extract was first washed with 10% HCl (5 ml) and then with water (2×10 ml). The washed extract was dried and evaporated to obtain 2-chloromethyl-5-chlorobenzofuran as a clear oil (yield: 0.5 g); HNMR (CDCl3, 60 MHz): 4.65 (s, 2H), 6.6 (s, 1H), 6.8-7.4 (m, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04939140
출처 데이터셋uspto-grants-1990_07
ORD IDord-74ec5ea09a564d7285053e9812c612c1
출처 메모uspto-grants-1990_07