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HRID 1109953作成日:2026年10月26日

Diethyl Ether → 4-[(S)-2-methylbutoxycarbonyl]phenyl 4-[(S)-2-propoxypropanoyloxy]benzoate

https://huagongshe.com/reaction/1109953

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物Benzoic acid, 4-hydroxy-, (2S)-2-methylbutyl esterHCID 13530950—
反応物4-[(S)-2-Propoxypropanoyloxy]benzoic acidHCID 14793534—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DichloromethaneHCID 6344—
生成物4-[(S)-2-methylbutoxycarbonyl]phenyl 4-[(S)-2-propoxypropanoyloxy]benzoateHCID 1484878774.1%

反応手順

In 12 ml of methylene chloride were dissolved 107 mg of 4-[2-(S)-propoxypropanoyloxy]benzoic acid, 95 mg of 4-[(S)-2-methyl butoxycarbonyl]phenol, and 140 mg of dicyclohexylcarbodiimide, and a catalytic amount of 4-dimethylaminopyridine was added to the solution, followed by stirring at room temperature. After 5 hours, diethyl ether was added to the reaction mixture, and any insoluble matter was removed by filtration. The filtrate was washed successively with a 10% hydrochloric acid aqueous solution, a saturated sodium bicarbonate aqueous solution, water, and a saturated sodium chloride aqueous solution, and dried over sodium sulfate. The solvent was removed from the residue by distillation, and the resulting oily substance was purified by silica gel column chromatography to obtain 139 mg of the entitled compound as a transparent oily substance. This compound did not crystalize even when allowed to stand at room temperature or less for a long time. The structure of the compound was confirmed by NMR and IR spectra.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05324451
出典データセットuspto-grants-1994_06
ORD IDord-4b8bae25343c46f4b7223d4db5d4d0e0
出典メモuspto-grants-1994_06