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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257450생성일: 2026년 10월 27일

Tetrahydrofuran → Methyl 4-[3-(3-bromophenyl)-1-cyanopropyl]benzoate

https://huagongshe.com/reaction/1257450

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물Methyl 4-(cyanomethyl)benzoateHCID 848548—
반응물3-Bromophenethyl bromideHCID 14361216—
반응물HCID 178418922HCID 178418922—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물Methyl 4-[3-(3-bromophenyl)-1-cyanopropyl]benzoateHCID 6693930055%

반응 단계

To a mixed solution of methyl 4-(cyanomethyl)benzoate (3.50 g, 20.0 mmol), tetrahydrofuran (25 mL) and N,N-dimethylformamide (10 ml) was added tert-butoxy potassium (2.69 g, 24.0 mmol) at −78° C., and the mixture was stirred for 30 min. To the reaction mixture was added 1-bromo-3-(2-bromoethyl)benzene (3.37 mL, 22.0 mmol) at the same temperature, and the mixture was stirred under ice-cooling for 4 hr. The reaction mixture was diluted with water, extracted with ethyl acetate, washed successively with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (carrier: silica gel, eluent: hexane-ethyl acetate) to give the title compound (3.94 g, 55%) as a colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461348B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-42dd959c09e7445aa431ff3d0d1e2b41
출처 메모uspto-grants-2013_06