関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | m-Anisoyl chloride | HCID 74374 | — |
| 反応物 | Lithium Bromide | HCID 82050 | — |
| 反応物 | 2-Bromo-4-chloro-6-fluorobenzonitrile | HCID 58579537 | — |
| 反応物 | HCID 178418546 | HCID 178418546 | — |
| 触媒 | Zinc | HCID 23994 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-Chloro-2-fluoro-6-(3-methoxybenzoyl)benzonitrile | HCID 58579524 | 55% |
反応手順
2-Bromo-4-chloro-6-fluorobenzonitrile (6.95 g, 29.64 mmol) was dissolved in THF (15 mL) and added to a bottle of Rieke® Zinc in THF (50 mg/mL, 50.0 mL, 38.24 mmol) at 0° C. under an argon atmosphere. The resulting mixture was stirred at rt for 6 h and then stored in a refrigerator for 60 h allowing the excess of zinc to settle. The solution was carefully decanted off and cooled to −78° C. under an argon atmosphere. A solution of lithium bromide (5.15 g, 59.28 mmol) and copper(I) cyanide (2.65 g, 29.64 mmol) in THF (30 mL) was added and the resulting mixture was stirred at rt for 30 min. The mixture was cooled to −78° C. and then 3-methoxybenzoyl chloride (4.17 mL, 29.64 mmol) was added dropwise. The cooling bath was removed and the resulting mixture was stirred at rt for 1.5 h. Saturated aqueous NH4Cl (12 mL) was added to the mixture, the THF was removed in vacuo and the residue was diluted with water (50 mL) and DCM (50 mL). The mixture was poured into a phase separator, the organic phase was collected, concentrated and purified on a silica gel column (0-30% EtOAc in heptane) to give 4.7 g (55%) of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08030500B2 |
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| 出典データセット | uspto-grants-2011_10 |
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| ORD ID | ord-e6852b5321c84dbb9f7c3449ee6208b3 |
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| 出典メモ | uspto-grants-2011_10 |
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