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HRID 579467作成日:2026年10月27日

Methanol → Ethyl 4-methoxy-3-oxobutanoate

https://huagongshe.com/reaction/579467

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物3-Bromo-7-hydroxy-4-methylchromen-2-oneHCID 5337545—
溶媒Hydrochloric AcidHCID 313—
生成物Ethyl 4-methoxy-3-oxobutanoateHCID 1264509915.1%

反応条件

温度0 °C

反応手順

NaH (7.71 g, 192.7 mmol) was suspended in DMF (110 mL). The solution of MeOH (2.64 g, 82.5 mmol) in DMF (55 mL) was added drop wise at 0° C. After that, the mixture was stirred at 0° C. for 30 min. The solution of compound 1 (9.54 g, 57.9 mmol) in DMF (55 mL) was added dropwise at 0° C., then the reaction mixture was allowed to warm slowly to RT and stirred for 16 h. The reaction mixture was diluted with 1N HCl (400 mL), extracted with MTBE (250 mL×3). The combined organic layer was washed with H2O (200 mL×5), dried over Na2SO4, filtered, concentrated, purified by silica gel column (PE:EA=10:1) afforded ethyl 4-methoxy-3-oxobutanoate (1.4 g, 15.1%) as light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040714B2
出典データセットuspto-grants-2015_05
ORD IDord-9e7544d2fee74e90bb23995b25649632
出典メモuspto-grants-2015_05