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HRID 1451作成日:2026年10月26日

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

https://huagongshe.com/reaction/1451

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6-ethoxycarbonyl-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 19690722—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物6-carboxy-5-methyl-2-phenyl-3-propargyl-4(3H)-pyrimidinoneHCID 1969071553.2%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726124
出典データセットuspto-grants-1998_03
ORD IDord-c70bc697c73a4481b3467e71a66893b5
出典メモuspto-grants-1998_03