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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1451생성일: 2026년 10월 25일

Sodium Hydroxide → 6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone

https://huagongshe.com/reaction/1451

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물6-ethoxycarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690722—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 1969071553.2%

반응 단계

To a solution of 1.81 g (6.1 mmol) of 6-ethoxycarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone in 100 mL of ethanol and 50 mL of THF was added 50 mL of 5% aqueous sodium hydroxide. The mixture was stirred at room temperature for 24 h and rotovapped to remove the bulk of the organic solvents. The residue was diluted with 50 mL of 5% aqueous sodium hydroxide and washed with 100 mL of ether. The aqueous phase was acidified with concentrated hydrochloric acid and extracted with two 100 mL portions of ethyl acetate. The combined ethyl acetate extracts were washed with 50 mL of brine, dried over MgSO4 and concentrated to leave 0.87 g (53%) of crude 6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinone as a brown oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726124
출처 데이터셋uspto-grants-1998_03
ORD IDord-c70bc697c73a4481b3467e71a66893b5
출처 메모uspto-grants-1998_03