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HRID 128784作成日:2026年10月26日

4-Hydroxybenzaldehyde → p-((Trimethylsilyl)oxy)benzaldehyde

https://huagongshe.com/reaction/128784

反応式

関与物質

役割名称HCID仕込み量
反応物4-HydroxybenzaldehydeHCID 126—
反応物ChlorotrimethylsilaneHCID 6397—
反応物TriethylamineHCID 8471—
溶媒Diethyl EtherHCID 3283—
生成物p-((Trimethylsilyl)oxy)benzaldehydeHCID 70536—

反応手順

Triethylamine (42 ml) is added dropwise to a stirred solution of 4-hydroxybenzaldehyde (33.5 g) and chlorotrimethylsilane (42 ml) in ether (300 ml). After 15 min, the mixture is filtered through diatomaceous earth and the filtrate is concentrated and distilled in vacuo, providing 4-(trimethylsiloxy)benzaldehyde as a colorless oil (43 g). This material is reacted with methoxymethyl triphenylphosphonium chloride and potassium tert-butoxide in THF, using the procedure described in Example 1 (A) above, to provide 1-(2-methoxyethenyl)-4-(trimethylsiloxy)benzene (35%) as a colorless oil after distillation in vacuo, as a mixture of (E) and (Z) isomers. This material (3.0 g) is dissolved in methanol (30 ml) containing methanesulfonic acid (0.4 ml), and the solution is refluxed for 3 hr. Sodium bicarbonate (8 ml of 1.0N solution) is added, and the mixture is concentrated in vacuo. The residue is taken up in ethyl acetate, dried, and concentrated to provide 4-[(2,2-dimethoxy)ethyl]phenol as a pale red oil (2.4 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05464865
出典データセットuspto-grants-1995_11
ORD IDord-37274ef06ac5448cba0b03217495d634
出典メモuspto-grants-1995_11