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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 404856생성일: 2026년 10월 26일

Dodecylbenzenesulphonic acid → 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol

https://huagongshe.com/reaction/404856

반응식

참여 물질

역할이름HCID투입량
반응물Dodecylbenzenesulphonic acidHCID 25457—
반응물1-(4-Trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthaleneHCID 68855880—
반응물3,4-Dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthaleneHCID 86619960—
용매TolueneHCID 1140—
생성물2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-olHCID 67172141—

반응 단계

The products from Step 4 (1-(4-trifluoromethylphenyl)-2-(dimethylhydroxymethyl)-4-hydroxy-6,7-dimethoxynaphthalene and 1-(3,4-dimethoxyphenyl-2-(dimethylhydroxymethyl)-4-hydroxy-6-trifluoromethylnaphthalene, 51.7 grams) were placed in a reaction flask equipped with a Dean-Stark trap and 775 mL of toluene was added. The reaction mixture was stirred under a nitrogen atmosphere and dodecylbenzene sulfonic acid (8.3 grams) was added. The reaction mixture was heated to reflux for 5 hours. Upon cooling to room temperature the reaction mixture was concentrated by rotary evaporation. The resulting brown solid was slurried in 300 mL of 15% ethyl acetate/85% hexanes. The solid was collected by vacuum filtration yielding 35.1 grams of 2,3-dimethoxy-7,7-dimethyl-9-trifluoromethyl-7H-benzo[C]fluoren-5-ol. This material was not purified further but was used directly in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08748634B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-d1c4b3dd9dc94c4ab28ce429096708c3
출처 메모uspto-grants-2014_06