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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 929110생성일: 2026년 10월 26일

Ethyl orthoformate → 3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenol

https://huagongshe.com/reaction/929110

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl orthoformateHCID 31214—
반응물Neopentyl glycolHCID 31344—
반응물6-Bromo-2-hydroxy-3-methoxybenzaldehydeHCID 262237—
촉매p-Toluenesulfonic acidHCID 6101—
생성물3-Bromo-2-(5,5-dimethyl-[1,3]dioxan-2-yl)-6-methoxy-phenolHCID 59761836100%

반응 조건

온도110 °C

반응 단계

A mixture of 6-bromo-2-hydroxy-3-methoxy-benzaldehyde (2.31 g, 10.0 mmol), neopentyl glycol (1.14 g, 11.0 mmol), TsOH (9.5 mg) and triethyl orthoformate (1.93 g, 13.0 mmol) were heated at 110° C. for 30 min and then partitioned between NaHCO3 (300 mL) solution and EtOAc (200 mL). The aqueous layer was extracted with EtOAc (3×30 mL) and the combined extracts were washed with brine and dried through Na2SO4. Evaporation of solvent afforded the title compound (3.17 g, 100%). 1H NMR (CDCl3) δ 0.85 (s, 3H), 1.27 (s, 3H), 3.70 (s, 2H), 3.82 (s, 2H), 3.85 (s, 3H), 5.90 (s, 1H), 6.72 (d, J=8 Hz, 1H), 7.02 (d, J=8 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09290503B2
출처 데이터셋uspto-grants-2016_03
ORD IDord-c1ede8de17c641598a8aca29cbf778de
출처 메모uspto-grants-2016_03