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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 255494생성일: 2026년 10월 24일

Sodium Hydroxide → 1-Pyrimid-2-yl-4-(4-chloro-phenyl)pyrazolin-5-one

https://huagongshe.com/ko/reaction/255494

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물Ethyl (4-chlorophenyl)acetateHCID 84177—
반응물2-HydrazinylpyrimidineHCID 346558—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물1-Pyrimid-2-yl-4-(4-chloro-phenyl)pyrazolin-5-oneHCID 1359053726.4%

반응 단계

19.9 g (0.1 mole) of ethyl 4-chloro-phenylacetate are heated at 100° C. with 23.8 g (0.2 mole) of dimethylformamide dimethyl acetal for 5 hours. All the volatile constituents are then distilled off at this temperature under a waterpump vacuum. The oily residue, which essentially consists of ethyl α-dimethylaminomethylene-4-chlorophenylacetate, is dissolved, without further purification, in 140 ml of ethanol. 11 g (0.1 mole) of 2-hydrazinopyrimidine and 10 ml of concentrated hydrochloric acid are added. The mixture is heated under reflux for 5 hours, cooled to room temperature and, after addition of 9 g of concentrated sodium hydroxide solution, stirred at room temperature for 5 hours. After neutralization with dilute hydrochloric acid, the mixture is diluted with 1 liter of water. The crystals which have separated out are filtered off with suction, washed with water and dried in air. 7.2 g (26.4% of theory) of 1-pyrimid-2-yl-4-(4-chloro-phenyl)pyrazolin-5-one are obtained. Melting point: 190° to 191° C. (methanol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04698344
출처 데이터셋uspto-grants-1987_10
ORD IDord-e456f43b817c4adf98a2f02c0b14dc07
출처 메모uspto-grants-1987_10