Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3,5-Di-tert-butyl-4-hydroxybenzoic acid → 4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3,5-Di-tert-butyl-4-hydroxybenzoic acid | HCID 15007 | — |
| 반응물 | N-Hydroxysuccinimide | HCID 80170 | — |
| 반응물 | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| 반응물 | 4-(3-Aminopropylthio)pyridine | HCID 15227695 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-[3-(3,5-Di-t-butyl-4-hydroxybenzoylamino)propylthio]pyridine | HCID 19079159 | 27.3% |
반응 단계
To a solution of 1.49 g (5.94 mmol) of 3,5-di-t-butyl-4-hydroxybenzoic acid and 889 mg (7.73 mmol) of N-hydroxysuccinimide in 60 ml of methylene chloride was added 1.38 g (7.13 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. Further 1.00 g (5.94 mmol) of 4-(3-aminopropylthio)pyridine was added and the mixture was stirred at rcom temperature for 8 hours. The reaction mixture was washed with water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 650 mg of the desired compound (27.3%, colorless powder), mp: 203.0°-204.0° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05246948 |
| 출처 데이터셋 | uspto-grants-1993_09 |
| ORD ID | ord-2c8dc63242cc44cab385e6bb518c6cff |
| 출처 메모 | uspto-grants-1993_09 |