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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29337생성일: 2026년 10월 23일

Water → Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate

https://huagongshe.com/ko/reaction/29337

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium percarbonateHCID 159762—
반응물Borane;tetrahydrofuranHCID 2723981—
반응물3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 68713160—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylateHCID 6871173580.6%

반응 단계

To a solution of 0.35 g (1.5 mmol) of 3-methyl-4-vinyl-1-benzofuran-2-carboxylate (Example 87, Step 1) in 3 mL of THF, cooled in an ice bath, was added 1 mL (1 mmol) of borane-THF complex (1.0M solution in THF). The reaction was stirred at room temperature for 2 hours. The reaction was cooled in an ice bath and 1.5 mL of water was added. Next 0.61 g of sodium percarbonate was added in one portion. The reaction was heated at ˜50° C. for 1 hour, then cooled to room temperature. Water was added and the resulting mixture was extracted with ethyl acetate. The organic layer washed with water and brine, dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was chromatographed on silica gel eluting with hexane/ethyl acetate (2:1) to provide 0.20 g of ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylate. Yield 54%. m.p. 88-90° C.; MS 249.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420001B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-965edae8814849798c651b63a638beac
출처 메모uspto-grants-2008_09