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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 745894생성일: 2026년 10월 25일

Fluorobenzene → 2-(4-Fluorobenzoyl)-naphthalene-3-carboxylic acid

https://huagongshe.com/reaction/745894

반응식

참여 물질

역할이름HCID투입량
반응물FluorobenzeneHCID 10008—
반응물Naphtho(2,3-c)furan-1,3-dioneHCID 69743—
반응물Aluminum(III) ChlorideHCID 6451240—
생성물2-(4-Fluorobenzoyl)-naphthalene-3-carboxylic acidHCID 23310940113.8%

반응 단계

45.0 g (227 mmol) of 2,3-naphthalenedicarboxylic acid anhydride are suspended in 200 ml (2.1 moles) of fluorobenzene. 75.5 g (565 mmol) of powdered aluminium chloride are added in the course of 5 minutes, with vigorous stirring (exothermic reaction up to about 32° C.). The dark red suspension is refluxed and stirred for 6 hours. The solution is then allowed to cool to room temperature and is poured onto about 500 g of ice, and is stirred to bring the hydrolysis to completion. Excess fluorobenzene is evaporated off and the resulting product is suspended in water. The suspension is filtered, the filtrate is rinsed with water and the product is dried. 76 g of crude 2-(4-fluorobenzoyl)-naphthalene-3-carboxylic acid are obtained. The crude product is stirred with 2 liters of 10% sodium carbonate solution, the resulting solution is acidified with hydrochloric acid and the white precipitate is filtered off and dried. 54.2 g (81% of theory) of 2-(4-fluorobenzoyl)-naphthalene-3-carboxylic acid are obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04601853
출처 데이터셋uspto-grants-1986_07
ORD IDord-0ff564ee45564632a2bab757242902bb
출처 메모uspto-grants-1986_07