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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 516944생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/516944

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참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Sodium IodideHCID 5238—
반응물6-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 339537—
반응물Sodium NitriteHCID 23668193—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
생성물6-iodo-3,4-dihydronaphthalen-1(2H)-oneHCID 4548980068.4%

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온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115054B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-c3c5a9c3e236430abd695b0db7c1139a
출처 메모uspto-grants-2015_08