関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hexane | HCID 8058 | — |
| 反応物 | 4-Chlorobenzophenone | HCID 8653 | — |
| 反応物 | 1-Phenethylimidazole | HCID 10219621 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | HCID 178519501 | HCID 178519501 | — |
反応手順
A solution of 20 ml. 20% butyl lithium in n-hexane (0.043 mol) in 30 ml. of diethyl ether was added dropwise under a nitrogen atmosphere to a solution of 5.5 g (0.032 mol) of 1-phenethylimidazole (J. Am. Chem. Soc., 71, 4000 (1949)) in 100 ml. of diethyl ether. After the addition was completed, the reaction mixture was stirred for another hour at room temperature. Then a solution of 7.8 g (0.036 mol) of 4-chlorobenzophenone in 75 ml. of anhydrous diethyl ether was added dropwise. The reaction mixture was stirred for 3 hours and it was then poured into 200 ml of ice-water. The ethereal layer was separated off, dried over sodium sulphate and the ether was distilled off. The residue was crystallised from a mixture of ethanol and petroleum ether (boiling range 40°-60° C.). α-(p-Chlorophenyl)-1-(phenethyl-α-phenylimidazole-2-methanol was obtained. Melting point 164°-165° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04152441 |
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| 出典データセット | uspto-grants-1979_05 |
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| ORD ID | ord-180ef7843d274bea8ebd175e969a1272 |
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| 出典メモ | uspto-grants-1979_05 |
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