関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-(Bromomethyl)benzonitrile | HCID 89599 | — |
| 反応物 | 5-Bromo-2-methoxybenzenethiol | HCID 11276017 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 2-(5-Bromo-2-methoxy-phenylsulfanylmethyl)-benzonitrile | HCID 22744853 | 64.9% |
反応手順
As depicted in Scheme 6, 162 mg (1.18 mmol) of anhydrous K2CO3 was added to a solution of 104 mg (0.470 mmol) of 2-methoxy-5-bromo-thiophenol in 5 mL of DMF, stirred for 15 minutes at 22° C. and 103 mg (0.520 mmol) of 2-bromomethyl-benzonitrile was added, then the reaction was capped and heated to 40° C. for 12 hours. The mixture was subsequently diluted with 5 mL of water, extracted with ethyl acetate (2×10 mL), and the organic extracts washed with water (3×10 mL), brine (2×10 mL), and dried (Na2SO4). The solvent was evaporated and the product was purified on silica gel (eluting with 9:1 of hexane/ethyl acetate) to afford 102 mg of the product as a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07375125B2 |
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| 出典データセット | uspto-grants-2008_05 |
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| ORD ID | ord-0628e9f3a74d4cf8b3fe8967a5c3285f |
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| 出典メモ | uspto-grants-2008_05 |
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