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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253245생성일: 2026년 10월 24일

Acetonitrile → Methyl 3,4-bis(2-methoxyethoxy)benzoate

https://huagongshe.com/ko/reaction/253245

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Potassium CarbonateHCID 11430—
반응물2-Bromoethyl methyl etherHCID 80972—
반응물Methyl 3,4-DihydroxybenzoateHCID 287064—
용매Ethyl AcetateHCID 8857—
생성물Methyl 3,4-bis(2-methoxyethoxy)benzoateHCID 4510817565%

반응 단계

To a mixture of methyl 3,4-dihydroxybenzoate (1.0 g, 6.0 mmol), potassium carbonate (3.3 g, 23.8 mmol) and acetonitrile (30 mL) was added 1-bromo-2-(methyloxy)ethane(1.7 mL, 17.9 mmol). The resulting mixture was heated at reflux 18 hour. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (100 mL), filtered and concentrated. The residue was then diluted with ethyl acetate (100 mL) and washed with 5% sodium hydroxide solution, water and brine (100 mL each), dried over sodium sulfate, filtered and concentrated to give an oily residue which was purified by flash chromatography (silica gel, 30%-50% ethyl acetate-hexane) to provide methyl 3,4-bis{[2-(methyloxy)ethyl]oxy}benzoate (1.1 g, 3.9 mmol, 65% yield). 1H NMR (400 MHz, CDCl3): 7.65-7.63 (d, 1H), 7.55 (s, 1H), 6.90-6.88 (d, 1H), 4.21-4.18 (m, 4H), 3.87 (s, 3H), 3.80-3.77 (m, 4H), 3.45 (s, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872014B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-9e68aa20b2194111be2538aea8212cfb
출처 메모uspto-grants-2011_01