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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1701068생성일: 2026년 10월 26일

Hydrochloric Acid → 2-Amino-3-oxo-3-phenylpropionic acid methylester

https://huagongshe.com/reaction/1701068

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Benzoyl chlorideHCID 7412—
반응물Methyl N-(diphenylmethylidene)glycinateHCID 563248—
반응물Potassium tert-butoxideHCID 23665647—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-3-oxo-3-phenylpropionic acid methylesterHCID 1329064880.9%

반응 조건

온도-78 °C

반응 단계

Dry tetrahydrofuran (250 ml) was cooled to −78° C. Potassium tert-butoxide (6.37 g; 56.72 mmol) was dissolved in dry tetrahydrofuran (100 ml) and added. (Benzhydrylideneamino) acetic acid methyl ester (14.35 g; 56.72 mmol) was added and the reaction mixture was stirred 30 min at −78° C. Benzoyl chloride (6.59 g; 56.72 mmol) was added dropwise and the reaction mixture was stirred 30 min at −78° C. Hydrochloric acid (1.0 M; 175 ml) was added dropwise. The reaction mixture was heated to room temperature and 2/3 of the solvent was removed in vacuo. Water (700 ml) was added and the reaction mixture was washed with diethyl ether (400 ml). The aqueous phase was evaporated in vacuo and the residue was dissolved in methanol and evaporated (2×150 ml). Methanol (80 ml) was added. The mixture was filtrated and the filtrate was evaporated in vacuo. The residue was recrystallised from tetrahydrofuran/diethyl ether to afford 8.86 g of 2-amino-3-oxo-3-phenylpropionic acid methylester as a hydrochloride.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06350767B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-ebf9ceb1d0964200b767543c0e77c089
출처 메모uspto-grants-2002_02