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1-(p-Tolyl)cyclopropanecarboxylic acid → 1-(4-Methyl-3-nitrophenyl)cyclopropane-1-carboxylic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 1-(p-Tolyl)cyclopropanecarboxylic acid | HCID 98639 | — |
| 反応物 | Nitronium tetrafluoroborate | HCID 11073463 | — |
| 溶媒 | Sulfolane | HCID 31347 | — |
| 生成物 | 1-(4-Methyl-3-nitrophenyl)cyclopropane-1-carboxylic acid | HCID 18400145 | — |
反応手順
Commercially available 1-(4-methylphenyl)-1-cyclopropane carboxylic acid is treated with nitronium tetrafluoroborate in sulfolane to afford 1-(4-methyl-3-nitrophenyl)-1-cyclopropane carboxylic acid. This is converted to 1-(4-methyl-3-nitrophenyl)-1-bromocyclopropane by treatment with mercuric oxide and bromine in methylene chloride. Reduction with zinc dust in the presence of calcium chloride in aqueous ethanol affords 5-cyciopropyl-2-methylaniline. Conversion to 4-cyclopropyl-5-(2-imidazolinylamino)-7-methylbenzimidazole is completed in the same manner as 4-ethyl-5-(2-imidazolinylamino)-7-methylbenzimidazole (see Example 2).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06486190B1 |
| 出典データセット | uspto-grants-2002_11 |
| ORD ID | ord-4f369910b121440998f40a296777283f |
| 出典メモ | uspto-grants-2002_11 |