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HRID 337320作成日:2026年10月26日

Isobutyronitrile → 2-(3-Bromo-5-fluorophenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/337320

反応式

関与物質

役割名称HCID仕込み量
反応物IsobutyronitrileHCID 6559—
反応物1-Bromo-3,5-difluorobenzeneHCID 136313—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物2-(3-Bromo-5-fluorophenyl)-2-methylpropanenitrileHCID 68845170100%

反応手順

At 2-5° C. a solution of lithium bis(trimethylsilyl)amide in THF (326 ml of 1 M, 326 mmol, 1.05 equiv.) was added dropwise into a solution of 1-bromo-3,5-difluorobenzene (60 g, 311 mmol, 1.0 equiv.) and isobutyronitrile (25.8 g, 373 mmol, 1.2 equiv.) in 360 mL of THF. After stirring for 20 h, 13% starting reagent remained so an additional 0.1 eq of lithium bis(trimethylsilyl)amide was added. After an additional 6 hr, 10% starting reagent remained so another 0.1 eq. of lithium bis(trimethylsilyl)amide and 0.1 eq. of isobutyronitrile were added. The reaction mixture was stirred overnight. The reaction mixture was quenched with a 1 N HCl solution, then concentrated down to remove some of the THF. The reaction mixture was extracted with methyl-tert-butyl ether (2 times) and concentrated under reduced pressure to get the crude product (75.3 g) which was used as is.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889682B2
出典データセットuspto-grants-2014_11
ORD IDord-3e7d74227a1f496ca8c5203918ba6d72
出典メモuspto-grants-2014_11