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HRID 35983作成日:2026年10月24日

Pyridine → 4,4-Dihydroxy-alpha-methylstilbene

https://huagongshe.com/ja/reaction/35983

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物(1,1'-Biphenyl)-2,3'-diolHCID 33665—
反応物4,4'-Dihydroxy-alpha-methylstilbeneHCID 656693—
溶媒1,4-DioxaneHCID 31275—
生成物4,4-Dihydroxy-alpha-methylstilbeneHCID 69933604—

反応条件

温度19 °C

反応手順

Trimellitic anhydride chloride (10.53 grams, 0.05 mole) and anhydrous 1,4-dioxane (400 milliliters) are added to a reactor and maintained under a nitrogen atmosphere with stirring to provide a solution. The resultant solution is cooled in an ice bath to 12° C., then a solution of 4,4'-dihydroxy-alpha-methylstilbene (5.66 grams, 0.05 hydroxyl equivalent), anhydrous 1,4-dioxane (50 milliliters) and pyridine (0.05 mole, 3.96 grams) is added dropwise to the reactor from a pressure equalizing addition funnel at a rate so as to maintain the temperature at 10°-12° C. The 4,4'-dihydroxy-alpha-methylstilbene used contains 98.8 area percent of the diphenol and 1.2 area percent of a single dimeric component as determined by high pressure liquid chromatographic analysis (uv detector set at 254 nm). After 70 minutes, addition of the solution is completed. After and additional 11 minutes, the ice bath cooling the reactor exterior is removed and the product slurry is allowed to warm to 19° C. over the next 236 minutes. The product slurry is filtered under a nitrogen atmosphere through a bed of diatomaceous earth with washing of the filter cake using anhydrous 1,4-dioxane (250 milliliters). The clear filtrate is concentrated to approximately 100 milliliters total volume via removal of 1,4-dioxane by rotary evaporation at 90° C. under vaccuum. The resultant slurry of crystalline product is held under a nitrogen atmosphere for 24 hours followed by filtration to recover the solid product. After drying in a vacuum oven at 100° C. and 1 mm Hg the product is recovered at a constant weight of 9.3 grams of light yellow colored powder. During the drying process, a minor amount of pyridine hydrochloride sublimed out of the product. Fourier transform infrared spectrophotometric analysis of a potassium chloride pellet of the product demonstrated the presence of anhydride carbonyl group absorbances (1868 and 1782 (with 1815 as a shoulder) cm-1) and the ester carbonyl group absorbance (1742 cm-1). Proton magnetic resonance spectroscopy additionally confirms the product structure.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05412057
出典データセットuspto-grants-1995_05
ORD IDord-c40b86b688064c119830878f5f36cdf4
出典メモuspto-grants-1995_05