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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1924822생성일: 2026년 10월 27일

Ethyl Bromide → 2-Ethyl-6-methylisonicotinic acid tert-butyl ester

https://huagongshe.com/reaction/1924822

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물MagnesiumHCID 5462224—
반응물2-Chloro-6-methyl-isonicotinic acid tert-butyl esterHCID 86040366—
반응물HCID 178418443HCID 178418443—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물2-Ethyl-6-methylisonicotinic acid tert-butyl esterHCID 67026967—

반응 단계

A solution of ethylmagnesiumbromide (freshly prepared from ethylbromide (392 mg, 3.6 mmol) and magnesium (83 mg, 3.4 mmol)) in Et2O (10 mL) is added to a cooled (−40° C.) and mechanically stirred solution of 2-chloro-6-methyl-isonicotinic acid tert-butyl ester (0.76 g, 3.34 mmol), Fe(acac)3 (21.2 mg, 0.06 mmol) and NMP (0.6 mL) in THF (60 mL). The mixture is warmed to rt during 0.5 h, diluted with Et2O (150 mL) and quenched with aq. KHSO4 (1 M, 40 mL). The phases are separated and the aq. phase is extracted with Et2O (2×50 mL). The combined organic extracts are dried (MgSO4), filtered and evaporated. The residue is purified by reversed phase MPLC to give 2-ethyl-6-methyl-isonicotinic acid tert-butyl ester; LC-MS: tR=0.67 min, [M+1]+=222.19; 1H NMR (CDCl3): δ 7.44 (s, 2H), 2.83 (q, J=7.6 Hz, 2H), 2.58 (s, 3H), 1.59 (s, 9H), 1.30 (t, J=7.6 Hz, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08178562B2
출처 데이터셋uspto-grants-2012_05
ORD IDord-c9aaad0c9712469f92d29d775a73a557
출처 메모uspto-grants-2012_05