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HRID 40351作成日:2026年10月26日

2-Methoxyethanol → Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate

https://huagongshe.com/reaction/40351

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethoxyethanolHCID 8019—
反応物TriphenylphosphineHCID 11776—
反応物Di-tert-butyl azodicarboxylateHCID 97268—
反応物Tert-butyl 2-(3-hydroxyquinolin-6-yl)acetateHCID 57691372—
溶媒BenzeneHCID 241—
溶媒Ethyl AcetateHCID 8857—
生成物Tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetateHCID 5769092582%

反応条件

温度0 °C

反応手順

A flask was charged with tert-butyl 2-(3-hydroxyquinolin-6-yl)acetate (581.04 mg, 2.241 mmol) and triphenylphosphine (1.175 g, 4.482 mmol) then sealed with a septum and an placed under N2. Benzene (10 mL) was added, followed by 2-methoxyethanol (0.8838 ml, 11.20 mmol). The heterogeneous solution was cooled to 0° C., and di-tert-butyl azodicarboxylate (1.032 g, 4.482 mmol) was added as a solid in a single portion. The solution was allowed to warm to rt and maintained 20 h. The solution was then partitioned between saturated aqueous. NH4Cl, and the layers separated. The aqueous layer was extracted with EtOAc (2×50 mL), and the combined organic layers were washed with brine, dried (MgSO4), and concentrated in vacuo. The resulting residue was purified by MPLC (Teledine Isco combiFlash Companion), 80 g SiO2, solvent system: 90:10 hexanes:EtOAc gradient to 50:50 hexanes:EtOAc to give tert-butyl 2-(3-(2-methoxyethoxy)quinolin-6-yl)acetate (585. 2 mg, 82% yield). LRMS (ESI) m/z calcd for C18H24NO4 (M+H) 318.2. found 318.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524900B2
出典データセットuspto-grants-2013_09
ORD IDord-8dfdfb4c74224e3191f4dafaaac5c262
出典メモuspto-grants-2013_09