Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Thiophene, 2,3,5-tribromo- → 3-Bromo-2,5-bis(4-(tert-butyl)phenyl)thiophene
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Thiophene, 2,3,5-tribromo- | HCID 76592 | — |
| 반응물 | 4-tert-Butylphenylboronic acid | HCID 2734320 | — |
| 반응물 | Sodium Carbonate Monohydrate | HCID 2735133 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-Bromo-2,5-bis(4-(tert-butyl)phenyl)thiophene | HCID 67973583 | 89% |
반응 단계
Sodium carbonate monohydrate (58.0 g, 468 mmol) was dissolved in water (500 mL) and a solution of 4-(tert-butyl)-phenylboronic acid (40.0 g) and 2,3,5-tribromothiophene (30.0 g, 94 mmol) in THF (500 mL) was added, and deoxygenated by bubbling with argon. Pd(PPh3)4 (5.0 g, 4.30 mmol) was added and the mixture refluxed for 24 h. The mixture was cooled and the aqueous phase separated and extracted with EtOAc. Organic fractions were combined washed with water (500 mL) and dried over MgSO4. The solvent was evaporated and the crude product washed in MeOH, filtered and dried overnight to afford a light yellow, powdery solid (35.46 g, 89%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US09176357B2 |
| 출처 데이터셋 | uspto-grants-2015_11 |
| ORD ID | ord-1995a93b609848b0a366d2f4f7a5bf92 |
| 출처 메모 | uspto-grants-2015_11 |