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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 359215생성일: 2026년 10월 26일

Hydrochloric Acid → Phenanthro[1,2-b]furan-2-methanol

https://huagongshe.com/reaction/359215

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TetrahydrofuranHCID 8028—
반응물Lithium borohydrideHCID 4148881—
반응물Ethyl phenanthro(1,2-b]furan-2-carboxylateHCID 12274414—
용매WaterHCID 962—
생성물Phenanthro[1,2-b]furan-2-methanolHCID 1477023990.3%

반응 단계

To a RB flask equipped with magnetic stirring bar, reflux condenser and N2 inlet tube with bubbler was added ethyl phenanthro[1,2-b]furan-2-carboxylate (H. G. Pars Pharmaceutical Laboratories, Inc., 7.9 g, 27.2 mmol), lithium borohydride (Aldrich, 0.65 g, 30 mmol) and dry THF (400 mL). The mixture was stirred at reflux for 6 h and then poured into H2O (1 L). The reaction mixture was acidified with 1N HCl and the resulting white solid was filtered, washed with additional H2O (1500 mL) then dissolved in CH2Cl2 (500 mL), dried (Na2SO4), filtered, concentrated to 200 mL and diluted to 500 mL with hexane. The resulting material was filtered, washed with hexane (100 mL) and placed in a vacuum oven overnight. A total of 6.1 g (90.1%) of phenanthro[1,2-b]-furan-2-methanol, mp 125°-126° , was obtained (C,H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04999369
출처 데이터셋uspto-grants-1991_03
ORD IDord-61e93e598362434f9130f8b2ebef0276
출처 메모uspto-grants-1991_03