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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 375690생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/375690

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Glycine methyl ester hydrochlorideHCID 122755—
반응물Methyl pentanimidateHCID 5743466—
용매MethanolHCID 887—
생성물2-Butyl-4-dimethylaminomethylene-2-imidazolin-5-oneHCID 13637557087%

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. 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05486617
출처 데이터셋uspto-grants-1996_01
ORD IDord-0076dd6527f64e80a23b59251d06709e
출처 메모uspto-grants-1996_01