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HRID 352451作成日:2026年10月27日

Hydrochloric Acid → 2-Methyl-4-(trifluoromethyl)benzonitrile

https://huagongshe.com/reaction/352451

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Potassium CyanideHCID 9032—
反応物Potassium CarbonateHCID 11430—
反応物4-Amino-3-methylbenzotrifluorideHCID 13750437—
反応物Sodium NitriteHCID 23668193—
触媒Copper sulfate pentahydrateHCID 24463—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
生成物2-Methyl-4-(trifluoromethyl)benzonitrileHCID 2225033288.4%

反応条件

温度5 °C

反応手順

Concentrated hydrochloric acid (16 mL) was added dropwise at a moderate rate to a heterogeneous mixture of 2-methyl-4-(trifluoromethyl)benzenamine (14 g, 80 mmol) and 120 mL of water while stirring vigorously. A thick suspension resulted which was stirred for 20 minutes, diluted with 280 mL of water and cooled to 5° C. A solution of sodium nitrite (5.5 g, 80 mmol) and 25 mL of water was added slowly to the reaction suspension. After stirring for 30 minutes at 5° C. a solution resulted which was stirred cold for 30 more minutes and then neutralized with potassium carbonate. This diazonium salt solution was then added portionwise via cannula to a stirred, 95° C. mixture of potassium cyanide (22 g, 0.34 mole), copper sulfate pentahydrate (20 g, 80 mmol) and 140 mL of water. After the addition the mixture was stirred for 30 minutes at 95° C. and then allowed to cool to room temperature. Ether was added and the heterogeneous mixture was filtered through celite. The solids were washed with ether, and the filtrate was partitioned. The aqueous phase was extracted with ether, and the combined organic extracts were dried over magnesium sulfate and concentrated under reduced pressure to afford 13.1 g of the title compound as brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747047B2
出典データセットuspto-grants-2004_06
ORD IDord-80d382ae0ee4470ebd58de5139c9de1c
出典メモuspto-grants-2004_06