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4-Bromobutyronitrile → 5-benzyl-3,4-dihydro-2H-pyrrole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Bromobutyronitrile | HCID 21412 | — |
| 反応物 | HCID 178419663 | HCID 178419663 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 5-benzyl-3,4-dihydro-2H-pyrrole | HCID 224018 | 132.6% |
反応手順
To a solution of 4-bromobutyronitrile (2.0 g, 13.5 mmol) in toluene (70 ml) was added 1.0 M benzylmagnesium bromide (20.0 ml, 20.0 mmol) in diethyl ether (70 ml) and the mixture was stirred for 2 hours at room temperature. The mixture was partitioned between 0.1N hydrochloric acid and ethyl acetate, and the organic layer was washed with aqueous sodium hydrogen carbonate, dried over sodium sulfate. The solvent was evaporated under reduced pressure to afford 5-benzyl-3,4-dihydro-2H-pyrrole (2.85 g). This compound was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08569294B2 |
| 出典データセット | uspto-grants-2013_10 |
| ORD ID | ord-9ed19ab4a3214edb8f98f66172edcdf8 |
| 出典メモ | uspto-grants-2013_10 |