関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 2,2-Dimethyl-2,3-dihydro-1-benzofuran-7-amine | HCID 91697 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 7-Amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran | HCID 53722008 | 83.3% |
反応手順
A stirred solution of 10.0 grams (0.061 mole) of 7-amino-2,3-dihydro-2,2-dimethylbenzofuran in 150 mL of N,N-dimethylformamide is cooled in an ice-water bath, and a solution of 10.9 grams (0.061 mole) of N-bromosuccinimide in 50 mL of N,N-dimethylformamide is added in one portion. Upon completion of addition, the reaction mixture is maintained in the ice-water bath for about one hour After this time the reaction mixture is poured into about 600 mL of water. The mixture is then extracted with two 200 mL portions of diethyl ether. The combined extracts are washed with two 100 mL portions of an aqueous 10% lithium chloride solution. The organic layer is dried with magnesium sulfate and filtered. The filtrate is concentrated under reduced pressure, yielding 12.3 grams of 7-amino-4-bromo-2,3-dihydro-2,2-dimethylbenzofuran. The NMR spectrum is consistent with the proposed structure.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05593998 |
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| 出典データセット | uspto-grants-1997_01 |
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| ORD ID | ord-d08210b56f49494ba7016092a97b7f32 |
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| 出典メモ | uspto-grants-1997_01 |
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