戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 58569作成日:2026年10月25日

Hydrochloric Acid → (R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid

https://huagongshe.com/reaction/58569

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物Ethoxalyl chlorideHCID 20884—
反応物phenylalaninol, (R)-HCID 853475—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物(R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acidHCID 6683188491%

反応手順

Triethylamine (0.703 mL; 5.01 mmol) was added to the mixture of (R)-2-amino-3-phenylpropan-1-ol (0.515 g; 3.34 mmol) and ethyl 2-chloro-2-oxoacetate (0.400 mL; 3.50 mmol) in dichloromethane (15 mL) at 0° C. After addition, the mixture was stirred at room temperature for 30 minutes, diluted with 40 mL of dichloromethane and washed successively with an aqueous solution of sodium carbonate and water. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. Water (5 mL) and a 2M solution of sodium hydroxide (5 mL; 10 mmol) were added to the resulting residue and the mixture was stirred at room temperature for 10 minutes. Water (10 mL) was added and the pH of the solution was adjusted to 1 by addition of a 6N hydrochloric acid. The formed precipitate was filtered off, and the filtrate was extracted with ethyl acetate (5×20 mL). The combined organic layers were dried over magnesium sulfate and evaporated to dryness to give 0.671 g (91%) of (R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acid as a white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09434722B2
出典データセットuspto-grants-2016_09
ORD IDord-24cbae80b894483981edd04cd2aeb457
出典メモuspto-grants-2016_09