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HRID 2387021作成日:2026年10月24日

3-Ethylphenol → 4-Ethyl-2-hydroxybenzaldehyde

https://huagongshe.com/ja/reaction/2387021

反応式

関与物質

役割名称HCID仕込み量
反応物3-EthylphenolHCID 12101—
反応物Methane, dichloromethoxy-HCID 21004—
触媒Titanium TetrachlorideHCID 24193—
生成物4-Ethyl-2-hydroxybenzaldehydeHCID 1023601765.3%

反応手順

Titanium(IV) chloride (100 mL, 100 mmol, 1M in CH2Cl2) followed by dichloromethyl methyl ether (7.47 mL, 82.5 mmol) was added to a cooled 0° C. solution of 3-ethylphenol (6.11 g, 50 mmol). The reaction mixture was stirred for 45 mins. The mixture was poured into ice and extracted with EtOAc. The organic layers were washed with brine, dried over Na2SO4 and concentrated to a bright pink oil. Purification by flash column chromatography (0% to 10% EtOAc in hexanes) gave 4-ethyl-2-hydroxy-benzaldehyde (4.9 g, 65%) followed by 2-ethyl-4-hydroxy-benzaldehyde (1.32 g, 18%). A: 1H NMR (400 MHz, CDCl3): δ 1.25 (t, J=7.6 Hz, 3 H), 2.67 (d, J=7.6 Hz, 2 H), 6.82 (s, 1 H), 6.85 (d, J=8.0 Hz, 1 H), 7.46 (t, J=8.0 Hz, 1 H), 9.83 (s, 1 H), 11.05 (s, 1 H). B: 1H NMR (400 MHz, CDCl3): δ 1.27 (t, J=7.6 Hz, 3 H), 3.03 (d, J=7.6 Hz, 2 H), 6.68 (s, 1 H), 6.78 (s, 1 H), 6.82 (d, J=8.3 Hz, 1 H), 7.77 (t, J=8.3 Hz, 1 H), 10.10 (s, 1 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08268835B2
出典データセットuspto-grants-2012_09
ORD IDord-521b495bb2af4e898272e25ab57e6c39
出典メモuspto-grants-2012_09