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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 352136생성일: 2026년 10월 24일

Diethyl Ether → [4-(2-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/352136

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물DiisopropylamineHCID 7912—
반응물2-MethoxypyridineHCID 74201—
반응물[2-(Methoxymethyl-carbamoyl)-ethyl]-carbamic acid tert-butyl esterHCID 86584230—
반응물HCID 178418348HCID 178418348—
용매TetrahydrofuranHCID 8028—
생성물[4-(2-Methoxy-pyridin-3-yl)-4-oxo-butyl]-carbamic acid tert-butyl esterHCID 102539314—

반응 조건

온도0 °C

반응 단계

2-Methoxypyridine (1.9 ml) and then diisopropylamine (0.1 ml) were added to a solution of methyl lithium (10 ml of a 1.6M solution in ether) in tetrahydrofuran (20 ml) at −78° C. and the solution was stirred at 0° C. for 18hand then re-cooled to −78° C. A solution of 1,1-dimethylethyl [3-(methoxymethylamino)-3-oxopropyl]-carbamate (1.6 g) in tetrahydrofuran (5 ml) was added slowly and the resultant solution was allowed to warm to −30° C. over 3.5 h, quenched with aqueous ammonium chloride and extracted with ether (three times). The combined organic extracts were dried (sodium sulphate), evaporated and purified by chromatography on silica eluting with petrol-ether gave the sub-title compound as a colourless oil (0.572 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06743939B2
출처 데이터셋uspto-grants-2004_06
ORD IDord-3e38315d28f442a38cbf626afe239183
출처 메모uspto-grants-2004_06