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HRID 1903873생성일: 2026년 10월 26일

Methane → 9H-Fluoren-9-one, 2-fluoro-

https://huagongshe.com/reaction/1903873

반응식

참여 물질

역할이름HCID투입량
반응물MethaneHCID 297—
반응물OxygenHCID 977—
반응물Benzyltrimethylammonium hydroxideHCID 66854—
반응물2-FluorofluoreneHCID 241132—
용매PyridineHCID 1049—
생성물9H-Fluoren-9-one, 2-fluoro-HCID 96016—

반응 단계

2-Fluorofluorene (824.7 g, 4.48 mol) was dissolved in pyridine (4 L) and stirred. A 40% solution of Triton B (100 mL of benzyltrimethylammonium hydroxide 40% in pyridine according to a general procedure of U. Sprinzak, J. Amer. Chem. Soc. 80 (1958) 5449) was added and oxygen was bubbled into the vigorously stirred solution. This exothermic reaction was run for 20 hours whereupon an additional portion of the Triton B solution (50 mL) was added with continued stirring and oxygen addition for an additional 24 hours. The resulting dark green reaction mixture was treated with Norite (100 g, neutralized charcoal), stirred for 30 minutes and filtered through a Celite pad (diatomaceous earth filter aid). The filter pad was then washed with pyridine (1 L). The combined filtrates were concentrated to a small volume in vacuo with heat. A 5% solution of hydrochloric acid in water (1 L) was added and the pyridine was azeotrophed in vacuo with heat. This process was repeated until a total of 6-8 L of water were evaporated. The granular product was filtered and washed with water (4 L) and air dried. The yellow-orange product was distilled through a large bore short path distillation apparatus (bp 167°-170° C.; 1.5 mm Hg) to yield into a chilled receiving flask the bright yellow 2-fluoro-9-fluorenone (600 g) with a m.p. 113°-115° C. and m/e+. 198 for C13H7FO.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04438272
출처 데이터셋uspto-grants-1984_03
ORD IDord-710d52f9d5f14f46b865fa466ffac0f8
출처 메모uspto-grants-1984_03