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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2179950생성일: 2026년 10월 26일

Ethyl Acetate → Tert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamate

https://huagongshe.com/reaction/2179950

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참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물2-BromothiazoleHCID 76430—
반응물[2-(Methoxymethyl-carbamoyl)-ethyl]-carbamic acid tert-butyl esterHCID 86584230—
반응물ButyllithiumHCID 178418339—
용매2-MethylpentaneHCID 7892—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl N-[3-oxo-3-(1,3-thiazol-2-YL)propyl]carbamateHCID 6980212267.1%

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온도0 °C

반응 단계

To a solution of 2-bromothiazole (5.035 g, 30.7 mmol) in dry tetrahydrofuran (125 ml) at −78° C. under nitrogen was added a solution of n-butyllithium in hexanes (1.6 M, 17.6 ml, 28.2 mmol) over a period of 30 minutes, followed by a solution of [3-(methoxymethylamino)-3-oxopropyl]carbamic acid 1,1-dimethylethyl ester (2.976 g, 12.8 mmol) in dry tetrahydrofuran (30 ml) added over 30 minutes. The reaction mixture was allowed to warm up to 0° C., quenched with saturated ammonium chloride and extracted with ethyl acetate (3×100 ml). The combined extracts were washed with water (3×50 ml) and saturated brine solution (1×100 ml), dried (magnesium sulphate) and concentrated in vacuo to leave a crude orange oil. Flash chromatography (silica, 25% ethyl acetate in isohexane) gave 2.2 g of a pale yellow oil (67%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06887871B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-81cd7b7aae524d368ae7775492dbbe36
출처 메모uspto-grants-2005_05