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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375693생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/375693

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물1,1-DibutoxytrimethylamineHCID 87683—
반응물Glycine methyl ester hydrochlorideHCID 122755—
반응물Methyl pentanimidateHCID 5743466—
용매MethanolHCID 887—
생성물2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 13637557089.9%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05486617
출처 데이터셋uspto-grants-1996_01
ORD IDord-5c3f369211f349648122080578b01ea9
출처 메모uspto-grants-1996_01