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HRID 2249373作成日:2026年10月26日

Bromomethyl methyl ether → 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene

https://huagongshe.com/reaction/2249373

反応式

関与物質

役割名称HCID仕込み量
反応物Bromomethyl methyl etherHCID 83093—
反応物1-Bromo-4-chloro-2-fluorobenzeneHCID 137275—
反応物Lithium diisopropylamideHCID 2724682—
溶媒TetrahydrofuranHCID 8028—
生成物1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzeneHCID 6880938171%

反応条件

温度-20 °C

反応手順

A solution of 1-bromo-4-chloro-2-fluorobenzene (20.4 g, 0.100 mol) in THF (50 mL) was slowly added to LDA (0.125 mol) in THF (600 mL) at −50° C. After addition the solution was warmed to −20° C. and then cooled to −50° C. a solution of bromomethoxymethane (25 g, 0.200 mol) in THF (25 mL) was slowly added and the reaction mixture was warmed to ambient temperature. The reaction was quenched with water (400 mL) and extracted with diethyl ether (2×150 mL). The combined organic phases were dried (sodium sulfate) and concentrated. The residual oil was distilled (70°-75° C./0.5 mm) to give 1-bromo-4-chloro-2-fluoro-3-methoxymethylbenzene (18.0 g, 0.071 mol): 1H NMR (CDCl3): δ 7.50 (m, 1H), 7.15 (dd, 1H), 4.65 (s, 1H), 3.40 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07314849B2
出典データセットuspto-grants-2008_01
ORD IDord-ac2da014daba480d85a8943209a2482b
出典メモuspto-grants-2008_01