関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Bromomethyl methyl ether | HCID 83093 | — |
| 反応物 | 1-Bromo-4-chloro-2-fluorobenzene | HCID 137275 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-Bromo-4-chloro-2-fluoro-3-(methoxymethyl)benzene | HCID 68809381 | 71% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07314849B2 |
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| 出典データセット | uspto-grants-2008_01 |
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| ORD ID | ord-ac2da014daba480d85a8943209a2482b |
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| 出典メモ | uspto-grants-2008_01 |
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