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HRID 356591作成日:2026年10月25日

Formaldehyde → 3beta-Hydroxymethoxy-androsten-17-one acetate

https://huagongshe.com/reaction/356591

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物DehydroepiandrosteroneHCID 5881—
反応物Acetyl chlorideHCID 6367—
反応物Sodium hydrideHCID 24758—
反応物Chloromethyl acetateHCID 69366—
触媒ZincchlorideHCID 3007855—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3beta-Hydroxymethoxy-androsten-17-one acetateHCID 131720942—

反応手順

To a solution of dehydroepiandrosterone (2.88 g, 10 mmol) in THF (100 mL) is added sodium hydride (11 mmol, 60% in oil) at room temperature under an argon atmosphere. When all the sodium hydride has reacted, chloromethyl acetate (prepared from acetyl chloride and formaldehyde (or derivative) using ZnCl2 as catalyst) is added and the mixture is heated for a few hours. After cooling, the mixture is poured into water and extracted with ethyl acetate. The organic phase is then washed with water, dried, filtered and evaporated to dryness to give the desired compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05837700
出典データセットuspto-grants-1998_11
ORD IDord-16c78ee6ebb64ca5bf1cc7df87333e49
出典メモuspto-grants-1998_11