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HRID 38712作成日:2026年10月25日

Potassium Carbonate → 4-(2-Acetoxyethoxy)-3-fluorobenzaldehyde

https://huagongshe.com/reaction/38712

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物1-Acetoxy-2-bromoethaneHCID 13564—
反応物3-Fluoro-4-hydroxybenzaldehydeHCID 587250—
溶媒AcetoneHCID 180—
溶媒Diethyl EtherHCID 3283—
生成物4-(2-Acetoxyethoxy)-3-fluorobenzaldehydeHCID 8717940651%

反応条件

温度55 °C

反応手順

A mixture of 3-fluoro-4-hydroxybenzaldehyde (2.0 g, 14.3 mmol), K2CO3 (5.92 g, 42.8 mmol) and 2-bromoethyl acetate (4.77 g, 28.5 mmol) in acetone (30 mL) is stirred at 55° C. for 24 h before it is diluted with diethyl ether (150 mL) and washed with water (3×50 mL). The organic extract is dried over MgSO4 and concetrated. The remaining residue is chromatographed on silica gel to give the title aldehyde (1.65 g) as a colourless oil. 1H NMR (CDCl3): δ 9.85 (s, 1H), 7.64-7.58 (m, 2H), 7.07 (t, J=8.2 Hz, 1H), 4.49-4.45 (m, 2H), 4.35-4.30 (m, 2H), 2.10 (s, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524752B2
出典データセットuspto-grants-2013_09
ORD IDord-d41d178f5d4941148a12d99a7d971dcf
出典メモuspto-grants-2013_09