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HRID 375692作成日:2026年10月24日

N,N,N-trimethyl-1,1-bis(1-methylethoxy)amine → 2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-one

https://huagongshe.com/ja/reaction/375692

反応式

関与物質

役割名称HCID仕込み量
反応物N,N,N-trimethyl-1,1-bis(1-methylethoxy)amineHCID 87682—
反応物2-butyl-3,5-dihydro-4H-imidazol-4-oneHCID 10909654—
溶媒DichloromethaneHCID 6344—
生成物2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 13637557077.1%

反応手順

A solution of 5.00 g (35.67 mmol) of 2-butyl-2-imidazolin-5-one and 7.02 g (39.24 mmol) of N,N-dimethylformamide diisopropyl acetal in 25 ml of methylene chloride was stirred at room temperature for 2.5 hours. Then, the solvent was removed on a Rotavapor, and the residue was treated with 40 ml of methylene chloride. The solution thus obtained was washed twice, each time with 10 ml of water, and dried (MgSO4) and concentrated on the Rotavapor. The residue was then dried in a high vacuum. 5.37 g of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one was obtained; the product had a content of greater than 90 percent, according to H-NMR. This corresponds to a yield of about 71 percent, based on the 2-butyl-2-imidazolin-5-one.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05486617
出典データセットuspto-grants-1996_01
ORD IDord-123c54209c5948949a04dc3581b0b0a2
出典メモuspto-grants-1996_01