돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1712197생성일: 2026년 10월 27일

Hydrochloric Acid → 2-Fluoro-4-(naphthalen-2-yl)benzaldehyde

https://huagongshe.com/reaction/1712197

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물N-FormylmorpholineHCID 20417—
반응물2-(3-Fluorophenyl)naphthaleneHCID 54238102—
반응물CID 53628100HCID 178418400—
용매TetrahydrofuranHCID 8028—
용매CyclohexaneHCID 8078—
생성물2-Fluoro-4-(naphthalen-2-yl)benzaldehydeHCID 5491245159.7%

반응 단계

A 86.86 ml cyclohexane solution of sec-butyl lithium in a concentration of 1.01M was dropped into a 300 ml THF solution of 15.00 g (=67.49 mmol) of 2-(3-fluorophenyl)naphthalene at −70° C. After the dropping was finished, the reaction solution was stirred at the same temperature for 1 hour, added with a 150 ml THF solution of 10.88 g (=94.49 mmol) of 4-formylmorpholine through dropping and then slowly heated to room temperature. After being stirred for 18 hours, 25 ml of 6N HCl(aq) was dropped into the reaction solution, and then the reaction mixture was extracted thrice with toluene. The extract was washed with water and an aqueous solution of NaHCO3, and then dried with anhydrous MgSO4. After the solvent was evaporated under a reduced pressure, the obtained yellow solid of 16.83 g was purified with silica gel chromatography using toluene as the eluent to obtain a yellowish solid of 13.26 g, which was further recrystallized with toluene to obtain 10.09 g of 2-fluoro-4-naphthalene-2-yl-benzaldehyde as yellowish crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07790915B2
출처 데이터셋uspto-grants-2010_09
ORD IDord-6fa4cf8be31045d09e1498835abfe99d
출처 메모uspto-grants-2010_09