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HRID 261958作成日:2026年10月26日
N,N,N',N'-Tetramethylethylenediamine → alpha-(o-tert.-Butylphenyl)-1-(methoxymethyl)-alpha-phenylimidazole-2-methanol
https://huagongshe.com/reaction/261958
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 反応物 | 1-(methoxymethyl)-1H-imidazole | HCID 88359 | — |
| 反応物 | (2-tert-Butylphenyl)(phenyl)methanone | HCID 54101900 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | alpha-(o-tert.-Butylphenyl)-1-(methoxymethyl)-alpha-phenylimidazole-2-methanol | HCID 12433889 | — |
反応手順
Under a nitrogen atmosphere and at -60° C., 38 ml. (0.08 mol) of a butyllithium solution (20% in n-hexane) were added drop-wise over the course of 45 minutes to a mixture of 9.6 g. (0.08 mol) of N,N,N',N'-tetramethylethylenediamine and 7 g. (0.06 mol) of 1-(methoxymethyl)imidazole in 100 ml. of anhydrous tetrahydrofuran. The mixture was stirred for another two hours under the same conditions and then 16 g (0.0675 mol) of o-tert.-butylbenzophenone in 100 ml. of anhydrous tetrahydrofuran were added dropwise. After the addition was completed, the mixture was stirred for 2 hours at -60° C., and one hour at room temperature. The mixture was decomposed with 5 ml. of water, the precipitate was filtered off and the filtrate was dried over sodium sulphate and concentrated. The solid residue was crystallised from isopropyl alcohol. α-(o-tert.-Butylphenyl)-1-(methoxymethyl)-α-phenylimidazole-2-methanol was obtained. Melting point 149°-150° 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-bcde5cfa3a484f71b99c2e2da89ec4cc |
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| 出典メモ | uspto-grants-1979_05 |
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