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HRID 2056738作成日:2026年10月26日

Trifluoroacetic acid → 6-bromo-1H,3H-naphtho[1,8-cd]pyran

https://huagongshe.com/reaction/2056738

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物TriethylsilaneHCID 12052—
反応物1H,3H-Naphtho(1,8-cd)pyran-1,3-dione, 6-bromo-HCID 66493—
反応物Sodium borohydrideHCID 4311764—
溶媒EthanolHCID 702—
生成物6-bromo-1H,3H-naphtho[1,8-cd]pyranHCID 69307283—

反応手順

To 6-bromo-1H,3H-naphtho[1,8-cd]pyran-1,3-dione (1.5 g, 5.4 mmol) in ethanol (10 mL) was added sodium borohydride (0.41 g, 10.8 mmol) and the mixture stirred at room temperature for 1 h. The reaction was quenched with 3M hydrochloric acid and extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The residue was dissolved in dichloromethane and trifluoroacetic acid (1.05 mL, 13.53 mmol) and triethylsilane (4.3 mL, 27 mmol) added. After stirring for 5 min at room temperature, the solvent was removed in vacuo and the residue purified by column chromatography on silica gel, eluting with dichloromethane, to yield 6-bromo-1H,3H-naphtho[1,8-cd]pyran as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07335660B2
出典データセットuspto-grants-2008_02
ORD IDord-93f7594914514440b42af07036f86d83
出典メモuspto-grants-2008_02