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HRID 37461作成日:2026年10月25日

Triethylamine → N-Boc-p-hydroxyphenylglycine

https://huagongshe.com/reaction/37461

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-(4-Hydroxyphenyl)glycineHCID 67149—
反応物O-(1,1-Dimethylethyl) S-(4,6-dimethyl-2-pyrimidinyl) carbonothioateHCID 148428—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物N-Boc-p-hydroxyphenylglycineHCID 21896684—

反応手順

To 33.4 g (0.2 mol) of p-hydroxyphenylglycine were added 110 ml of water, 42 ml (1.5 eq.) of triethylamine, 52.8 g (1.1 eq.) of S-t-butoxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine and 110 ml of dioxane, and the mixture was stirred at room temperature for 14 hours. To the reaction mixture was added 300 ml of water, and the mixture was extracted with 400 ml of ethyl acetate. The organic layer was extracted with 100 ml of a 5% aqueous solution of sodium hydrogencarbonate. The aqueous layers were combined, adjusted to pH 3 with 5N hydrochloric acid under ice-cooling and extracted with ethyl acetate. The organic layer was washed with an aqueous solution of potassium hydrogensulfate and a saturated aqueous solution of sodium chloride, and dried over magnesium sulfate. The solvent was distilled off. The thus-obtained crystals were collected by filtration with ethyl acetate/hexane. Yield: 46.0 g (86.1%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05420275
出典データセットuspto-grants-1995_05
ORD IDord-ebc2486f05974e7d85e113f967e5ed1d
出典メモuspto-grants-1995_05