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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 66104생성일: 2026년 10월 26일

Sodium hydride → 4-(1-Adamantyloxy)-3-fluoronitrobenzene

https://huagongshe.com/reaction/66104

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물1-AdamantanolHCID 64152—
반응물1,2-Difluoro-4-nitrobenzeneHCID 123053—
반응물HCID 178418361HCID 178418361—
용매BenzeneHCID 241—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-(1-Adamantyloxy)-3-fluoronitrobenzeneHCID 12510265171.6%

반응 단계

A mixture of 16 g (64 mmoles) of 1-adamantanol, 3.35 g (70 mmoles NaH) of 50% NaH in oil, 60 ml of benzene, and 60 ml of dimethylformamide is heated until hydrogen is vigorously evolved (80°). Heating is discontinued until the effervescence subsides, and then the mixture is heated at 90° for 0.5 hour. To this mixture cooled to 20° is added dropwise with stirring 9.7 g (63 mmoles) of 3,4-difluoronitrobenzene. A slight exotherm is observed, and the mixture is refluxed (110° ) for 64 hours. Water (300 ml) is added to the cooled mixture, and it is extracted with CH2Cl2 (200 ml). The CH2Cl2 layer is washed with water (3×300 ml), and the four separate wash water portions are extracted in succession with the same 200 ml of CH2Cl2. The combined organic layers are dried, and concentrated to give 31.5 g of solid crude product, which is chromatographed on silica gel (3100 g), eluting with CH2Cl2, and taking 500 ml fractions. Fractions 14 and 15 contain 12.6 g of white solid product, m.p. 110.1 - 118.2, as confirmed by nmr spectroscopy.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04130561
출처 데이터셋uspto-grants-1978_12
ORD IDord-21ef7129b2b049cfa976c53ea53dcb32
출처 메모uspto-grants-1978_12