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HRID 375693作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/375693

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1,1-DibutoxytrimethylamineHCID 87683—
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 13637557089.9%

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. Then, the mixture was stirred for 15 minutes. 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. 9.00 g (43.36 mmol) of N,N-dimethylformamide dibutyl acetal then was added, during the course of 5 minutes, and the reaction mixture was stirred for a further 3 hours. Then, the solvent was removed on the 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. The organic phase was dried (MgSO4), filtered and concentrated on the Rotavapor, and the residue was dried in a high vacuum. 6.92 g of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one was obtained; the product had a content of about 80 percent according to H-NMR. This corresponds to a yield of about 72 percent, based on the methyl pentanimidate.

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-5c3f369211f349648122080578b01ea9
出典メモuspto-grants-1996_01