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HRID 646999作成日:2026年10月25日

1-Bromo-3-chloropropane → 4-(3-Chloro-propoxy)-2-methyl-benzaldehyde

https://huagongshe.com/reaction/646999

反応式

関与物質

役割名称HCID仕込み量
反応物1-Bromo-3-chloropropaneHCID 8006—
反応物Potassium CarbonateHCID 11430—
反応物4-Hydroxy-2-methylbenzaldehydeHCID 458185—
反応物4-(3-Iodo-propoxy)-2-methyl-benzaldehydeHCID 57434758—
溶媒AcetonitrileHCID 6342—
生成物4-(3-Chloro-propoxy)-2-methyl-benzaldehydeHCID 5743475982%

反応条件

温度65 °C

反応手順

4-(3-Iodo-propoxy)-2-methyl-benzaldehyde. 1-Bromo-3-chloropropane (5.03 g, 32.0 mmol, 1.0 equiv) was added to a solution of 2-methyl-4-hydroxybenzaldehyde (4.35 g, 32.0 mmol, 1.0 equiv) and K2CO3 (8.8 g, 64.0 mmol, 2.0 equiv) in acetonitrile (75 mL). The mixture was heated at 65° C. for 16 h, then cooled to rt and filtered through diatomaceous earth. The filtrate was concentrated and the residue was purified by column chromatography (silica gel, 10% ethyl acetate in hexanes) to afford 5.58 g (82%) of 4-(3-chloro-propoxy)-2-methyl-benzaldehyde. To a refluxing solution of 4-(3-chloro-propoxy)-2-methyl-benzaldehyde in acetone (100 mL), KI (58 g) was added portion wise over 3 d. The mixture was cooled to rt and water was added. The aqueous mixture was extracted three times with ethyl acetate and the combined extracts were dried (Na2SO4), filtered, and concentrated. The residue was purified by column chromatography (silica gel, 5% ethyl acetate in hexanes) to afford 6.13 g (77%) of the title compound. 1H NMR (400 MHz, CD3OD): 10.1 (s, 1H), 7.75 (d, J=8.6 Hz, 1H), 6.84 (dd, J=8.6, 2.5 Hz, 1H), 6.74 (d, J=2.2 Hz, 1H), 4.11 (t, J=5.8 Hz, 2H), 3.36 (t, J=6.7 Hz, 2H), 2.65 (s, 3H), 2.29 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07705143B2
出典データセットuspto-grants-2010_04
ORD IDord-e72cecdcf3724e13993ec06635186fcc
出典メモuspto-grants-2010_04