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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1275871생성일: 2026년 10월 26일

Hydrochloric Acid → 9-Methylene-9H-fluorene

https://huagongshe.com/reaction/1275871

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참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물9-(Acetoxymethyl)fluoreneHCID 540179—
반응물Potassium tert-butoxideHCID 23665647—
용매Diethyl EtherHCID 3283—
생성물9-Methylene-9H-fluoreneHCID 7814794%

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온도5 °C

반응 단계

A 1000 mL flask was charged with 9-acetoxymethylfluorene (30.0 g, 126 mmol) and anhydrous petroleum ether (bp 35-60° C., 400 mL, Aldrich) and it was cooled to 5° C. Solid potassium tert-butoxide (16.0 g, 142 mmol, Aldrich) was added in one portion. After stirring for 6 hours, the mixture was poured into dilute HCl (200 mL, 0.1 N). Et2O was added (100 mL); the layers were separated and the product extracted into Et2O (2×100 mL). Combined organic portions were dried over anhydrous MgSO4 and the solvent was removed via rotary evaporation. The crude product dibenzofulvene was isolated as a yellow solid (21.3 g, 94% yield, >99% pure by GC). Further purification was accomplished by recrystallization from petroleum ether, to yield dibenzofulvene in the form of white needles (Tm 51.5-53° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06162937
출처 데이터셋uspto-grants-2000_12
ORD IDord-54f4cf02a21b4680a27a9e5b6e869325
출처 메모uspto-grants-2000_12