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p-Bromochlorobenzene → (4-chlorophenyl)[4-(1H-imidazol-1-yl)phenyl]methanol
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | p-Bromochlorobenzene | HCID 7806 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | 4-(1H-imidazol-1-yl)benzaldehyde | HCID 736530 | — |
| 反応物 | Magnesium | HCID 5462224 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | (4-chlorophenyl)[4-(1H-imidazol-1-yl)phenyl]methanol | HCID 3789353 | 83.9% |
反応手順
A Grignard reagent which is prepared by reacting 1.9 g of magnesium with 15 g of p-chlorobromobenzene in 40 ml of ether is added to a suspension of 6.2 g of 4-(1-imidazolyl)benzaldehyde in 70 ml of ether at 0° C. After the mixture is stirred at room temperature for an hour, the reaction mixture is poured into an aqueous ammonium chloride solution with caution. The mixture is extracted with chloroform and the chloroform is distilled off. The residue is purified column-chromatographically and recrystallized from toluene to give 8.6 g of α-(4-chlorophenyl)-4-(1-imidazolyl)benzenemethanol as white crystals, melting at 148.5°-149.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04581369 |
| 出典データセット | uspto-grants-1986_04 |
| ORD ID | ord-d34700e522374180804b1117911452f5 |
| 出典メモ | uspto-grants-1986_04 |