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HRID 1094298作成日:2026年10月25日

Benzyl Bromide → 4-Benzyloxy-3-ethyl-5-methylbenzaldehyde

https://huagongshe.com/reaction/1094298

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Potassium CarbonateHCID 11430—
反応物2-Ethyl-6-methylphenolHCID 519333—
反応物3-Ethyl-4-hydroxy-5-methylbenzaldehydeHCID 23159210—
反応物HCID 178436626HCID 178436626—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物4-Benzyloxy-3-ethyl-5-methylbenzaldehydeHCID 86639348—

反応条件

温度60 °C

反応手順

To a solution of 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (34.9 g, 0.213 mol, prepared from 2-ethyl-6-methyl-phenol according to the literature cited for 3-ethyl-4,N-dihydroxy-5-methyl-benzamidine) in acetonitrile (350 mL), K2CO3 (58.7 g, 0.425 mol) and benzylbromide (36.4 g, 0.213 mol) is added. The mixture is stirred at 60° C. for 2 h before it is cooled to rt, diluted with water and extracted twice with EA. The org. extracts are washed with water and concentrated to give crude 4-benzyloxy-3-ethyl-5-methyl-benzaldehyde (45 g) as an orange oil. 1H NMR (CDCl3): δ 1.29 (t, J=7.5 Hz, 3H), 2.40 (s, 3H), 2.77 (q, J=7.8 Hz, 2H), 4.90 (s, 2H), 7.31-7.52 (m, 5 H), 7.62 (d, J=1.5 Hz, 1H), 7.66 (d, J=1.8 Hz, 1H), 9.94 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08133910B2
出典データセットuspto-grants-2012_03
ORD IDord-7d14cba212c2442c95d563ddc363546a
出典メモuspto-grants-2012_03