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HRID 40182作成日:2026年10月24日

Tetrahydrofuran → Ethyl 3-(7-methoxyquinolin-4-yl)propanoate

https://huagongshe.com/ja/reaction/40182

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物Tri-tert-butylphosphine tetrafluoroborateHCID 2734635—
反応物4-Chloro-7-methoxyquinolineHCID 10607829—
反応物HCID 178471816HCID 178471816—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Ammonium HydroxideHCID 14923—
生成物Ethyl 3-(7-methoxyquinolin-4-yl)propanoateHCID 67503802—

反応手順

4-chloro-7-methoxyquinoline (0.35 g, 2 mmol), tri-t-butylphosphonium tetrafluoroborate (0.05 g, 0.2 mmol), and tris(dibenzylideneacetone)dipalladium (0) (0.08 g, 0.09 mmol) were combined. The reaction vessel was purged and flushed with nitrogen three times, followed by addition of 3-ethoxy-3-oxopropylzinc bromide in THF (10 mL, 5 mmol, 0.5 M). The reaction mixture was microwaved at 150° C. for 60 minutes. Upon completion, ammonium hydroxide (10 mL) was added. After 30 minutes the mixture was filtered and the filtrate was partitioned between water and ethyl acetate. Extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried over magnesium sulfate, and concentrated. Purified by MPLC with a gradient of 20 to 50% EtOAc in CH2Cl2. (ESI, pos. ion) m/z: 354.1 (M+H).

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-2749dc371527437e9924f4eb2acea80b
出典メモuspto-grants-2013_09