Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Aniline → 2-Norbornylphenylamine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Aniline | HCID 6115 | — |
| 반응물 | Bicyclo(2.2.1)heptan-2-one | HCID 10345 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | HCID 178418385 | HCID 178418385 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 2-Norbornylphenylamine | HCID 54125158 | 106.9% |
반응 단계
In a 250 mL flask equipped with a Dean-Start separator, the following mixture is brought to reflux: 9.3 g of aniline, 12.1 g 2-norbornanone, 13.2 g benzotriazole and 120 mL xylene. After 16 h, the mixture is reduced to dryness, then it is solubilized in 300 mL methanol, and the product is reduced with 6 g NaBH4 at 50° C. for 1 h. The mixture is then poured into 200 mL water and the organic product is extracted with 3×100 mL toluene. The organic phase is recovered, dried over magnesium sulfate, and then reduced to dryness. In this manner, 20 g of the desired amine are produced.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06030555 |
| 출처 데이터셋 | uspto-grants-2000_02 |
| ORD ID | ord-cae0fbda27d04fde94c95b484282019f |
| 출처 메모 | uspto-grants-2000_02 |