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HRID 29337作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Sodium percarbonateHCID 159762—
反応物Borane;tetrahydrofuranHCID 2723981—
反応物3-Methyl-4-vinylbenzofuran-2-carboxylic acid ethyl esterHCID 68713160—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl 4-(2-hydroxyethyl)-3-methyl-1-benzofuran-2-carboxylateHCID 6871173580.6%

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420001B2
出典データセットuspto-grants-2008_09
ORD IDord-965edae8814849798c651b63a638beac
出典メモuspto-grants-2008_09