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HRID 1735501作成日:2026年10月25日

Sodium Hydroxide → 2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-one

https://huagongshe.com/reaction/1735501

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium HydroxideHCID 14798—
反応物Dimethylformamide dimethyl acetalHCID 78373—
反応物Glycine methyl ester hydrochlorideHCID 122755—
反応物Methyl pentanimidateHCID 5743466—
溶媒MethanolHCID 887—
生成物2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 13637557087%

反応手順

5.00 g (39.42 mmol) of glycine methyl ester hydrochloride was added in a single portion to a solution of 1.59 g (39.42 mmol) of sodium hydroxide in 13 ml of methanol at 0° C. The temperature dropped to -10° C. The mixture was then stirred for 15 minutes and during this time the temperature rose again to 0° C. 4.73 g (39.42 mmol) of methyl pentanimidate was added, and the mixture was stirred at room temperature for 3 hours. Then, during the course of 5 minutes, 5.62 g (43.39 mmol) of N,N-dimethylformamide dimethyl acetal was added, and the reaction mixture was stirred for a further 3 hours. Thereafter, solvent was removed on a Rotavapor, and the residue was treated with 40 ml of CH2Cl2 and 15 ml of water. After phase separation, the organic phase was washed with 10 ml of water, and then the combined H2O phases were washed twice, each time with 20 ml of CH2Cl2. Then, the combined organic phases were dried (MgSO4), filtered, concentrated on the Rotavapor and dried in a high vacuum. 6.70 g of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one was obtained, having a content of about 90 percent, according to 1H-NMR. This corresponds to a yield of about 78 percent, based on the methyl pentanimidate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05536841
出典データセットuspto-grants-1996_07
ORD IDord-b2d424266a7a4b348073595357cdfde2
出典メモuspto-grants-1996_07