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HRID 343303作成日:2026年10月26日

2-Formyl-17beta-estradiol → 3-Hydroxyestra-1,3,5(10)-trien-17-one-2-carboxaldehyde

https://huagongshe.com/reaction/343303

反応式

関与物質

役割名称HCID仕込み量
反応物2-Formyl-17beta-estradiolHCID 9994980—
反応物Jones' reagentHCID 131709961—
溶媒AcetoneHCID 180—
生成物3-Hydroxyestra-1,3,5(10)-trien-17-one-2-carboxaldehydeHCID 1140378662%

反応手順

To a solution of 3,17β-dihydroxyestra-1,3,5(10)-triene-2-carboxaldehyde (2a, 0.300 g, 1.0 mmol) in acetone (20 mL) was added Jones reagent (0.5 mL) at 0° C. The reaction mixture was stirred for 5 min, then quenched with 2-propanol, and extracted with EtOAc. The combined organic layers were washed with H2O, then with saturated aqueous NaCl, and dried (MgSO4). The desiccant was filtered and the solvent was evaporated at reduced pressure. The residue was purified by column chromatography (silica gel) using n-hexane:THF (4:1→3:1, v/v) to approximately 0.185 g of 5 (62% yield), m.p. 154°-157° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05861388
出典データセットuspto-grants-1999_01
ORD IDord-a8501990f77f478391e18e93927f23a9
出典メモuspto-grants-1999_01