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HRID 352283作成日:2026年10月25日

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

https://huagongshe.com/reaction/352283

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Trimethyl borateHCID 8470—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-Bromo-4-propylbenzeneHCID 136374—
反応物MagnesiumHCID 5462224—
反応物6-Bromo-2-(3,4-difluorophenyl)-1,2,3,4-tetrahydronaphthaleneHCID 22709043—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-(3,4-Difluorophenyl)-6-(4-propylphenyl)-1,2,3,4-tetrahydronaphthaleneHCID 22709053—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06746728B1
出典データセットuspto-grants-2004_06
ORD IDord-ae4514c24a244888b6d3cb4fd123196c
出典メモuspto-grants-2004_06