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HRID 516944作成日:2026年10月26日

Sulfuric Acid → 6-iodo-3,4-dihydronaphthalen-1(2H)-one

https://huagongshe.com/reaction/516944

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuric AcidHCID 1118—
反応物Sodium IodideHCID 5238—
反応物6-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 339537—
反応物Sodium NitriteHCID 23668193—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物6-iodo-3,4-dihydronaphthalen-1(2H)-oneHCID 4548980068.4%

反応条件

温度0 °C

反応手順

To a stirred clear solution of 6-amino-3,4-dihydronaphthalen-1(2H)-one (15 g, 93 mmol) in acetic acid (150 mL) and water (150 mL) was added sulfuric acid (5.5 mL, 101 mmol) dropwise at 0° C. A solution of sodium nitrite (12.90 g, 187 mmol) in water (100 mL) was then added dropwise over 40 min at the same temperature. The mixture was stirred at 0° C. for 10 min before being added to a stirred solution of sodium iodide (55.8 g, 372 mmol) in water (600 mL) slowly over 2 h at 0° C. The resulting brown suspension was stirred at 0° C. for 30 min and at room temperature for 1 h. The mixture was extracted with ethyl acetate (400 mL, 2×100 mL). The combined ethyl acetate extracts were washed with water (60 mL), saturated aqueous Na2S2O3 solution until the brown color disappeared, and saturated aqueous K3PO4 (60 mL) solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. Flash chromatography purification (330 g silica gel column, gradient elution from 5 to 15% ethyl acetate in hexanes) afforded 6-iodo-3,4-dihydronaphthalen-1(2H)-one (17.3 g, 63.6 mmol) as a solid. LC/MS M+1=273.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115054B2
出典データセットuspto-grants-2015_08
ORD IDord-c3c5a9c3e236430abd695b0db7c1139a
出典メモuspto-grants-2015_08