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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

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物1-(methoxymethyl)-1H-imidazoleHCID 88359—
反応物(2-tert-Butylphenyl)(phenyl)methanoneHCID 54101900—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-(o-tert.-Butylphenyl)-1-(methoxymethyl)-alpha-phenylimidazole-2-methanolHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US04152441
出典データセットuspto-grants-1979_05
ORD IDord-bcde5cfa3a484f71b99c2e2da89ec4cc
出典メモuspto-grants-1979_05