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Tetrahydrofuran → 7-bromo-4-methyl-1H-indole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 4-Bromo-3-nitrotoluene | HCID 79224 | — |
| 反応物 | HCID 178418507 | HCID 178418507 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 7-bromo-4-methyl-1H-indole | HCID 18752862 | — |
反応手順
1 l (1 mol) of a tetrahydrofuran solution containing 1.0 M vinylmagnesium bromide was added to a tetrahydrofuran solution (300 ml) containing 65.0 g (301 mmol) of 2-bromo-5-methylnitrobenzene at −60° C. under stirring for one hour in nitrogen atmosphere. An aqueous saturated ammonium chloride and ethyl acetate were added to the reaction mixture solution, and the insoluble matters were filtered off. The filtrate was dried over magnesium sulfate and concentrated. Then, the residue was purified by silica gel column chromatography, to give 35.5 g of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07834049B2 |
| 出典データセット | uspto-grants-2010_11 |
| ORD ID | ord-dfbab5c697244738928f3dd8cc579791 |
| 出典メモ | uspto-grants-2010_11 |