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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 355754생성일: 2026년 10월 24일

Acetic Acid → ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate

https://huagongshe.com/ko/reaction/355754

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Ethyl 4-(aminomethyl)benzoateHCID 436161—
반응물2-(Benzyloxy)-5-bromobenzaldehydeHCID 733087—
반응물Sodium borohydrideHCID 4311764—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoateHCID 22675503—

반응 단계

2-Benzyloxy-5-bromobenzaldehyde and ethyl 4-aminomethylbenzoate were heated together at 100° C. for 1 hour. The mixture was cooled, dissolved in ethanol (100 ml) and sodium borohydride (1.3 g) was added. The mixture was stirred for 18 hours at ambient temperature, acidified with acetic acid and water (200 ml) was added. The mixture was extracted with diethyl ether (4×100 ml), the extracts washed with saturated aqueous NaHCO3, dried (MgSO4), filtered and evaporated to give ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate which was purified by chromatography on silica gel eluting with CH2Cl2 then 5% ethyl acetate/CH2Cl2 (yield 11.4 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05834468
출처 데이터셋uspto-grants-1998_11
ORD IDord-ac2592b1d7e9403f99739f686d9d8a9c
출처 메모uspto-grants-1998_11