Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 3,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 1-(Bromomethyl)naphthalene | HCID 137844 | — |
| 반응물 | 4,5-Dichloroimidazole | HCID 140018 | — |
| 반응물 | 1,3,5-Tris(bromomethyl)benzene | HCID 530258 | — |
| 생성물 | 3,3',3''-(benzene-1,3,5-triyltris(methylene))tris(4,5-dichloro-1-(naphthalen-1-ylmethyl)-1H-imidazol-3-ium) bromide | HCID 86719746 | — |
반응 단계
4,5-dichloroimidazole (3.00 g, 21.90 mmol) was dissolved in THF and brought to reflux. Potassium hydroxide (2.46 g, 43.80 mmol) was added to the solution and allowed to reflux for 30 min. 1,3,5-tris(bromomethyl)benzene (2.61, 7.30 mmol) was added to the solution and refluxed overnight. Solution was filtered while hot to remove the KBr precipitate and the filtrate returned to reflux. 1-(bromomethyl)naphthalene (4.84 g, 21.90 mmol) was added to the solution and refluxed for 3 h. The volatiles were removed in vacuo and the resulting waxy yellow solid was washed in ethyl ether. A resulting product will be collected and analyzed.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09278951B2 |
| 출처 데이터셋 | uspto-grants-2016_03 |
| ORD ID | ord-a82ad7559bce4983b97eac21cd1f30bb |
| 출처 메모 | uspto-grants-2016_03 |