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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 58569생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/58569

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물Ethoxalyl chlorideHCID 20884—
반응물phenylalaninol, (R)-HCID 853475—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(R)-2-(1-hydroxy-3-phenylpropan-2-ylamino)-2-oxoacetic acidHCID 6683188491%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434722B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-24cbae80b894483981edd04cd2aeb457
출처 메모uspto-grants-2016_09