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HRID 1258839作成日:2026年10月24日

HCID 67115761、化合物 → acetic acid (2R,3R,4R,5S,6S)-3,4,5-triacetoxy-6-[3-(3-amino-4-hydroxy-benzyl)-4-chloro-phenyl]-tetrahydro-pyran-2-ylmethyl ester

https://huagongshe.com/ja/reaction/1258839

反応式

関与物質

役割名称HCID仕込み量
反応物HCID 67115761HCID 67115761—
触媒IronHCID 23925—
溶媒Acetic AcidHCID 176—
生成物acetic acid (2R,3R,4R,5S,6S)-3,4,5-triacetoxy-6-[3-(3-amino-4-hydroxy-benzyl)-4-chloro-phenyl]-tetrahydro-pyran-2-ylmethyl esterHCID 6711589679.5%

反応条件

温度60 °C

反応手順

To a stirred solution of acetic acid (2R,3R,4R,5S,6S)-3,4,5-triacetoxy-6-[4-chloro-3-(4-hydroxy-3-nitro-benzyl)-phenyl]-tetrahydro-pyran-2-ylmethyl ester (1.71 g, 2.9 mmol) in glacial acetic acid (15 mL) was added iron powder (3.22 g, 57.7 mmol). After stirring at 60° C. for 15 min, the reaction mixture was filtered through a celite bed. The filtrate was concentrated under reduced pressure, and the resulting residue was taken up in ethyl acetate and the solution was washed with water, saturated aqueous sodium bicarbonate solution, and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated to a residue which was purified by silica gel column chromatography to furnish acetic acid (2R,3R,4R,5S,6S)-3,4,5-triacetoxy-6-[3-(3-amino-4-hydroxy-benzyl)-4-chloro-phenyl]-tetrahydro-pyran-2-ylmethyl ester (1.3 g)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08466114B2
出典データセットuspto-grants-2013_06
ORD IDord-f5556b0f3fa9447aabf3042307f536a7
出典メモuspto-grants-2013_06