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HRID 1868668作成日:2026年10月27日

Bis(2-bromoethyl) ether → 4-(3-Methoxyphenyl)oxane-4-carbonitrile

https://huagongshe.com/reaction/1868668

反応式

関与物質

役割名称HCID仕込み量
反応物Bis(2-bromoethyl) etherHCID 21521—
反応物Sodium hydrideHCID 24758—
反応物(3-Methoxyphenyl)acetonitrileHCID 88310—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物4-(3-Methoxyphenyl)oxane-4-carbonitrileHCID 1878636693.5%

反応条件

温度0 °C

反応手順

A mixture of NaH (3.2 g, 79 mmol) in 50 mL NMP stirred at 0° C., was treated dropwise with a mixture of 2-(3-methoxyphenyl)acetonitrile (3.9 g, 26 mmol) and 1-bromo-2-(2-bromoethoxy)ethane (6.1 g, 26 mmol) in 20 mL. The mixture was allowed to warm to room temperature and stirred for 15 hours, M+1=218. The mixture was then carefully quenched with 100 mL H2O and the pH was adjusted to 5. The mixture was extracted with ether (3×100 mL). The combined organic layers were washed with H2O (3×50 mL) and brine (20 mL). The organic layer was dried over anhydrous Na2SO4, concentrated in vacuo, and purified by column chromatography eluting with 10-20% EtOAc/hexane to give 5.28 g of the crude product 5.28 g as a pale yellow oil. MS (m/z)=218 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07635715B2
出典データセットuspto-grants-2009_12
ORD IDord-b3c61d16b4bf41a7a9fc7033fef635f9
出典メモuspto-grants-2009_12