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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 128784생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/128784

반응식

참여 물질

역할이름HCID투입량
반응물4-HydroxybenzaldehydeHCID 126—
반응물ChlorotrimethylsilaneHCID 6397—
반응물TriethylamineHCID 8471—
용매Diethyl EtherHCID 3283—
생성물p-((Trimethylsilyl)oxy)benzaldehydeHCID 70536—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05464865
출처 데이터셋uspto-grants-1995_11
ORD IDord-37274ef06ac5448cba0b03217495d634
출처 메모uspto-grants-1995_11