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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 410611생성일: 2026년 10월 26일

Methyl iodide → Tert-butyl 2-methyl-2-(1,3-thiazol-2-yl)propanoate

https://huagongshe.com/reaction/410611

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물2-ChlorothiazoleHCID 76429—
반응물tert-Butyl propionateHCID 88561—
반응물Sodium bis(trimethylsilyl)amideHCID 2724254—
용매TolueneHCID 1140—
생성물Tert-butyl 2-methyl-2-(1,3-thiazol-2-yl)propanoateHCID 6725869162%

반응 조건

온도0 °C

반응 단계

Toluene (30 mL) was placed in a nitrogen-flushed flask and degassed with nitrogen (20 min). 2-Chlorothiazole (900 mg, 7.53 mmol) and tert-butyl propionate (1.176 g, 9.03 mmol) were added, and the mixture was cooled to 0° C. NaHMDS (0.6 M in toluene, 30.1 mL, 18.06 mmol) was added. The reaction was stirred for 2 h at 0° C., allowed to warm to room temperature, and stirred for 18 h at room temperature. Methyl iodide (3.85 g, 27.1 mmol) was then added. After 1 h at room temperature, the orange reaction was quenched (under nitrogen) with aqueous saturated NH4Cl. The mixture was extracted with ethyl acetate (2×), and the combined organic layers were washed with brine, dried (Na2SO4), filtered and evaporated. Flash chromatography (0-25% ethyl acetate in hexanes) afforded tert-butyl 2-methyl-2-(1,3-thiazol-2-yl)propanoate (1.06 g, 62%) as a pale yellow oil. MS ESI: [M+H]+ m/z 228.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759366B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-bb82558b31444071a7821cc07a9db13c
출처 메모uspto-grants-2014_06