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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130707생성일: 2026년 10월 26일

Hydrochloric Acid → 2-(4-Methoxyphenyl)-2-methylpropanenitrile

https://huagongshe.com/reaction/130707

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물IsobutyronitrileHCID 6559—
반응물4-FluoroanisoleHCID 9987—
반응물Potassium bis(trimethylsilyl)amideHCID 3251421—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Methoxyphenyl)-2-methylpropanenitrileHCID 21916652%

반응 단계

Add potassium bis(trimethylsilyl)amide (39.90 g, 200 mmol) to a stirred solution of 4-fluoroanisole (15.0 mL, 133 mmol), isobutyronitrile (49.0 mL, 539 mmol) and anhydrous tetrahydrofuran (150 mL). Heat the reaction to reflux under nitrogen for 72 h. Cool the reaction to room temperature, pour it into 1 N hydrochloric acid (300 mL), and extract with diethyl ether (3×100 mL). Wash the diethyl ether extracts with brine (100 mL), dry the extracts over magnesium sulfate, filter, and concentrate on a rotary evaporator to give the crude product. The crude product is purified by flash chromatography on silica gel eluting with 10% ethyl acetate/hexanes to yield 12.13 g (52%) of 2-(4-methoxy-phenyl)-2-methyl-propionitrile: TLC: Rf in 10% ethyl acetate/hexanes: 0.30; 1H NMR (CDCl3): 7.40-7.37 (m, 2H), 6.92-6.90 (m, 2H), 3.81 (s, 3H), 1.70 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-ccf243a42fc24f19b931160a3d67fead
출처 메모uspto-grants-2008_06