돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 422549생성일: 2026년 10월 23일

Tetrahydrofuran → Ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoate

https://huagongshe.com/ko/reaction/422549

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물N-methyl-2-pyrrolidoneHCID 13387—
반응물Ethyl 3-(1-chlorophthalazin-6-yl)-4-methylbenzoateHCID 59726010—
반응물HCID 178418573HCID 178418573—
촉매Ferric acetylacetonateHCID 5483663—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoateHCID 59726018—

반응 단계

A 150-ml round-bottom flask under argon was charged with ethyl 3-(1-chlorophthalazin-6-yl)-4-methylbenzoate (358 mg, 1096 μmol), iron(III) acetylacetonate (38.7 mg, 109.6 □mol), THF (4200 μl), and 1-methyl-2-pyrrolidinone (420 μl). Methylmagnesium bromide (1.4M solution in toluene/tetrahydrofuran (75:25); 1174 μl, 1643 μmol) was then added via a syringe to the resulting orange red suspension, causing an immediate color change to brown, and finally to violet. The resulting mixture was stirred for 10 min, and the reaction (which remained a suspension) was diluted with EtOAc and carefully quenched with a few drops of 10% aqueous HCl solution. The mixture was washed with saturated aqueous NaHCO3 solution and the organic layer was dried (MgSO4), filtered, and concentrated in vacuo. CombiFlash purification (20% to 90% EtOAc in Hexanes) afforded ethyl 4-methyl-3-(1-methylphthalazin-6-yl)benzoate as a light golden brown oil. MS (ES+): 307.1 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101612B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-e452b98d6b1042638a46b3596af5928a
출처 메모uspto-grants-2012_01