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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 408577생성일: 2026년 10월 24일

Chloroacetaldehyde → 2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester

https://huagongshe.com/ko/reaction/408577

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetaldehydeHCID 33—
반응물Acetic AcidHCID 176—
반응물Sulfuric acid magnesium salt (1:1)HCID 24083—
반응물Ethyl 2-(benzylamino)propanoateHCID 222273—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매DichloromethaneHCID 6344—
생성물2-[Benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl esterHCID 70557779—

반응 조건

온도0 °C

반응 단계

To a solution of 2-benzylamino-propionic acid ethyl ester (1 eq.) in dry DCM was added MgSO4 (0.75 eq.). The reaction was cooled to 0° C. then the above solution of chloroacetaldehyde in dry DCM (solution I) and acetic acid (1 eq.) were added. Sodium triacetoxyborohydride (1.5 eq.) was added portionwise. The reaction was stirred for 1 h at 0° C. The crude was carefully quenched with a saturated aqueous solution of NaHCO3. Then aqueous NaOH (2N) was added. The aqueous layer was extracted with DCM. The combined organic layers were washed with an aqueous saturated solution of NaHCO3, then dried over MgSO4 and concentrated under reduced pressure. The crude was purified by chromatography on silica gel (elution with heptane/EtOAc 98/2 to 95/5) to afford 2-[benzyl-(2-chloro-ethyl)-amino]-propionic acid ethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08759334B2
출처 데이터셋uspto-grants-2014_06
ORD IDord-ebec0e38facf4fb582b154836ae73339
출처 메모uspto-grants-2014_06