Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 259855생성일: 2026년 10월 26일
Triethylamine → 4-(2-Chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinoline
https://huagongshe.com/reaction/259855
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 3,5-Di-tert-butyl-4-hydroxybenzoic acid | HCID 15007 | — |
| 반응물 | 3-Amino-4-(2-chlorophenyl)-6,8-dimethylquinoline | HCID 10446536 | — |
| 반응물 | Diethylphosphorylcyanide | HCID 13586794 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(2-Chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinoline | HCID 15230624 | 24.2% |
반응 단계
To a mixture of 3-amino-4-(2-chlorophenyl)-6,8-dimethylquinoline (1.02 g), 3,5-di-tert-butyl-4-hydroxy benzoic acid (750 mg), diethylphosphoryl cyanide (DEPC) (587 mg) and N,N-dimethylformamide (100 mg) was dropwise added a solution of triethylamine (0.51 ml) in DMF (2 ml) under stirring at 0° C. The mixture was stirred at 0° C. for 30 minutes and at room temperature for one night. Then, the mixture was diluted with water and extracted with ethyl acetate. The ethyl acetate layer was concentrated after being washed with water and dried (MgSO4). The residue was purified by a silica gel column chromatography with hexane-ethyl acetate (85:15,V/V), and then crystallized from methanol to give 4-(2-chlorophenyl)-3-(3,5-di-tert-butyl-4-hydroxybenzamido)-6,8-dimethylquinoline (373 mg, 24.2%). Recrystallization from methanol gave colorless prisms of mp 127°-129° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05523407 |
|---|
| 출처 데이터셋 | uspto-grants-1996_06 |
|---|
| ORD ID | ord-2893b047d4754530ab361116f9b20703 |
|---|
| 출처 메모 | uspto-grants-1996_06 |
|---|