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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352283생성일: 2026년 10월 24일

Hydrochloric Acid → 2-(3,4-Difluorophenyl)-6-(4-propylphenyl)-1,2,3,4-tetrahydronaphthalene

https://huagongshe.com/ko/reaction/352283

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Trimethyl borateHCID 8470—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물1-Bromo-4-propylbenzeneHCID 136374—
반응물MagnesiumHCID 5462224—
반응물6-Bromo-2-(3,4-difluorophenyl)-1,2,3,4-tetrahydronaphthaleneHCID 22709043—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(3,4-Difluorophenyl)-6-(4-propylphenyl)-1,2,3,4-tetrahydronaphthaleneHCID 22709053—

반응 조건

온도80 °C

반응 단계

A solution of 4.5 g of 4-propylphenylboric acid obtained by reaction of a Grignard reagent prepared from 4-propylbromobenzene and magnesium with trimethoxy borane and subsequent hydrolysis with dilute hydrochloric acid, 5.0 g of 6-bromo-2-(3,4-difluorophenyl)-1,2,3,4-tetrahydronaphthalene synthesized in the example 15, 0.3 g of tetrakis(triphenylphosphine)palladium(0), and 3.0 g of potassium phosphate in 30 ml of dimethyl formamide was stirred for 10 hours at 80° C. The mixture was subsequently cooled to room temperature, water was added, and the mixture was extracted with toluene. The organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate, and then concentrated. The residue was purified by silica gel column chromatography (hexane) and then recrystallized from ethanol, and yielded 4 g of 2-(3,4-difluorophenyl)-6-(4-propylphenyl)-1,2,3,4-tetrahydronaphthalene. This compound displayed a purity of 99.7% when analyzed by gas chromatography, and had a molecular weight of 362.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06746728B1
출처 데이터셋uspto-grants-2004_06
ORD IDord-ae4514c24a244888b6d3cb4fd123196c
출처 메모uspto-grants-2004_06