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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 429378생성일: 2026년 10월 24일

Acetonitrile → 3-Iodobenzoylacetonitrile

https://huagongshe.com/ko/reaction/429378

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물DiisopropylamineHCID 7912—
반응물TetrahydrofuranHCID 8028—
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 4-iodobenzoateHCID 142891—
반응물Lithium diisopropylamideHCID 2724682—
반응물ButyllithiumHCID 178418339—
생성물3-IodobenzoylacetonitrileHCID 11623179—

반응 조건

온도-50 °C

반응 단계

n-Butyllithium (30.5 ml, 76 mmol, 2.5 M solution in hexane) was added dropwise to a cooled (0° C.) solution of diisopropylamine (10.6 ml, 76 mmol) in 10 ml dry tetrahydrofuran. Once addition was complete, the solution was kept at 0° C. for 10 minutes and was then cooled to −50° C. This cold LDA solution was then added to a −50° C. solution of acetonitrile (2.37 ml, 45.3 mmol) and ethyl 4-iodobenzoate (10.0 g, 36.2 mmol) in dry tetrahydrofuran (18 ml). Once addition was complete, the reaction was stirred at −50° C. for 3 hours and was subsequently warmed to 0° C. Saturated ammonium chloride was added (20 ml) and the reaction mixture was allowed to warm to room temperature. The product was extracted into ether and washed with 1N hydrochloric acid (50 ml). The organics were washed with brine (50 ml), dried over MgSO4 and then concentrated in vacuo to a red oil. The oil was purified through a small plug of silica gel using 3:1-2:1 hexanes/ethyl acetate as eluent. Concentration of the column fractions in vacuo gave 2-(3-iodobenzoyl)-acetonitrile (8.3 g) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06316466B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-d6290a6681f043c48b6439088d503c6f
출처 메모uspto-grants-2001_11