Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Nitrophenol → tert-Butyldimethyl(4-nitrophenoxy)silane
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Nitrophenol | HCID 980 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | tert-Butyldimethyl(4-nitrophenoxy)silane | HCID 532659 | 100% |
반응 단계
4-Nitrophenol (5.6 g, 40 mmol) was dissolved in CH2Cl2 (200 ml) and stirred at room temperature in the presence of tertbutyldimethyl-silyl chloride (7.8 g, 52 mmol), 4-dimethylaminopyridine (0.1 g, 0.8 mmol) and triethylamine (7.2 ml, 52 mmol). After 30 minutes at room temperature, the reaction mixture was washed with H2O (2×200 ml) and the resulting aqueous phases were extracted with CH2Cl2 (100 ml). The combined organic phases were dried over Na2SO4 and concentrated. The residue was chromatographed over silica gel (hexane-ether 9:1) to provide tert-Butyl-dimethyl-(4-nitro-phenoxy)-silane (10 g, 100%) as a yellow solid, m.p. 36°-38° C. and MS: m/e=253 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05889026 |
| 출처 데이터셋 | uspto-grants-1999_03 |
| ORD ID | ord-f731cdad91b249178cadff74b1ee40cb |
| 출처 메모 | uspto-grants-1999_03 |