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HRID 1275905作成日:2026年10月24日

2-[2,4-Dimethylphenyl]-4,5-dihydro-4,4-dimethyloxazole → 4,5-Dihydro-4,4-dimethyl-2-[4-methyl-2-[2-[2,3-dimethylphenyl]ethyl]phenyl]oxazole

https://huagongshe.com/ja/reaction/1275905

反応式

関与物質

役割名称HCID仕込み量
反応物2-[2,4-Dimethylphenyl]-4,5-dihydro-4,4-dimethyloxazoleHCID 22117273—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物4,5-Dihydro-4,4-dimethyl-2-[4-methyl-2-[2-[2,3-dimethylphenyl]ethyl]phenyl]oxazoleHCID 22117204—

反応手順

n-Butyllithium (6.9 ml of a 2.5M soln in hexanes) was added dropwise to the product of example 21 step (i) (3.51 g) in tetrahydrofuran (60 ml) at -78° C. After 2 hours the product from step (i) (3.45 g) was added. After 1 hour the solution was left to warm to room temperature. The solution was quenched with water and extracted with ethyl acetate. The organic solution was dried (MgSO4) and evaporated under reduced pressure. Yield 1.83 g.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06162808
出典データセットuspto-grants-2000_12
ORD IDord-91762cdd6cfb4b918869ccc2090b8faa
出典メモuspto-grants-2000_12