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HRID 1836798作成日:2026年10月27日

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

https://huagongshe.com/reaction/1836798

反応式

関与物質

役割名称HCID仕込み量
反応物Chloromethyl Methyl EtherHCID 7864—
反応物TetrahydrofuranHCID 8028—
反応物DiisopropylethylamineHCID 81531—
反応物3-Bromo-6-methoxybenzene-1,2-diolHCID 3705874—
溶媒WaterHCID 962—
生成物1-Bromo-2,3-bis(methoxymethyloxy)-4-methoxy-benzeneHCID 1056662791%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06777578B2
出典データセットuspto-grants-2004_08
ORD IDord-7754d388b453470ca553b337dfea0fb0
出典メモuspto-grants-2004_08