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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1836798생성일: 2026년 10월 26일

Chloromethyl Methyl Ether → 1-Bromo-2,3-bis(methoxymethyloxy)-4-methoxy-benzene

https://huagongshe.com/reaction/1836798

반응식

참여 물질

역할이름HCID투입량
반응물Chloromethyl Methyl EtherHCID 7864—
반응물TetrahydrofuranHCID 8028—
반응물DiisopropylethylamineHCID 81531—
반응물3-Bromo-6-methoxybenzene-1,2-diolHCID 3705874—
용매WaterHCID 962—
생성물1-Bromo-2,3-bis(methoxymethyloxy)-4-methoxy-benzeneHCID 1056662791%

반응 단계

To a solution of 1-bromo-2,3-dihydroxy-4-methoxy-benzene (5.0 g) and anhydrous tetrahydrofuran (20 mL) at 0° C. under argon was added diisopropylethylamine (8.0 mL). The solution was stirred for 15 min, methyloxymethyl chloride (3.5 mL) was added, and the reaction mixture stirred for 3 hours. The solution was poured into water (250 mL), extracted with dichloromethane and the solvent removed in vacuo to provide an orange oil. The oil was purified by flash column chromatography (hexane-ethyl acetate, 2:1) to yield a clear oil (6.4 g, 91%): EIMS m/z 308 (M+, 81Br), 306 (M+, 79Br), 232, 230, 45; IR (neat, cm−1) vmax 2963, 2836, 1221, 1159, 1084, 966; 1H NMR δ 7.25 (1H, d, J=9.0 Hz, H5), 6.61 (1H, d, J=9.0 Hz, H4), 5.20 (2H, s, OCH2), 5.13 (2H, s, OCH2), 3.84 (3H, s, OCH3), 3.66 (3H, s, OCH3), 3.59 (3H, s, OCH3); 13C—NMR (75.5 MHZ) δ 153.31, 148.24, 140.05, 127.49, 108.94, 108.73, 99.39, 98.73, 58.14, 57.46, 56.11. Anal. Calcd. For C11H15O5Br: C, 43.02; H, 4.92. Found: C, 42.86; H, 4.93.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06777578B2
출처 데이터셋uspto-grants-2004_08
ORD IDord-7754d388b453470ca553b337dfea0fb0
출처 메모uspto-grants-2004_08