Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Ethyl 4-(aminomethyl)benzoate | HCID 436161 | — |
| 반응물 | 2-(Benzyloxy)-5-bromobenzaldehyde | HCID 733087 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | ethyl 4-[N-(2-benzyloxy-5-bromobenzyl)aminomethyl]benzoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05834468 |
| 출처 데이터셋 | uspto-grants-1998_11 |
| ORD ID | ord-ac2592b1d7e9403f99739f686d9d8a9c |
| 출처 메모 | uspto-grants-1998_11 |