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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1047391생성일: 2026년 10월 27일

Hydrochloric Acid → 2-Docosyloxy-9-(4-chlorophenyl)-9-fluorenol

https://huagongshe.com/reaction/1047391

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물2-Docosyloxy-9-fluorenoneHCID 66719005—
반응물HCID 178478191HCID 178478191—
용매TetrahydrofuranHCID 8028—
생성물2-Docosyloxy-9-(4-chlorophenyl)-9-fluorenolHCID 4692772288%

반응 단계

Under a nitrogen atmosphere, 2-docosyloxy-9-fluorenone (250 mg, 0.50 mmol) prepared in the above-mentioned 1-1 was suspended in THF (2.5 ml), and dissolved at 50° C. 4-Chlorophenylmagnesium bromide solution was added dropwise, and the mixture was stirred. After completion of the reaction, the reaction mixture was cooled to room temperature, 1N hydrochloric acid was added dropwise thereto in a water bath until foaming stopped to quench the reaction. The mixture was extracted with chloroform (15 ml), and washed 3 times with 1N hydrochloric acid (5 ml), 3 times with 5% NaHCO3 solution (5 ml), and once with 20% NaCl solution (5 ml). The organic layer was dried over Na2SO4, and the solvent of the filtrate was evaporated. The obtained residue was isolated and purified by silica gel column chromatography, and precipitated with methanol (3 ml) to give 2-docosyloxy-9-(4-chlorophenyl)-9-fluorenol (270 mg, 0.44 mmol, 88%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569453B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-58aa747319a14635a26188dc5f11af86
출처 메모uspto-grants-2013_10