Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → 4-(t-Butyldiphenylsilyloxy)-1-methyl-1-butanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | Pentane-1,4-diol | HCID 79083 | — |
| 반응물 | tert-Butyldiphenylchlorosilane | HCID 94078 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(t-Butyldiphenylsilyloxy)-1-methyl-1-butanol | HCID 23028571 | — |
반응 단계
In N,N-dimethylformamide (200 ml) were dissolved 1,4-pentanediol (10.0 g, 96.0 mmol) and imidazole (6.6 g, 96.9 mmol). Under ice cooling, t-butyl chlorodiphenylsilane (25.2 ml, 96.4 mmol) was added dropwise. After completion of the dropwise addition, the reaction mixture was stirred at room temperature for 2 days. To the reaction mixture was added diethyl ether, followed by washing with water. The organic layer was dried over anhydrous magnesium sulfate. After filtration, the residue obtained by concentrating the filtrate under reduced pressure was purified by silica gel chromatography (hexane:ethyl acetate=5:1), whereby the title compound (32.0 g, 97%) was obtained as a colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07399775B2 |
| 출처 데이터셋 | uspto-grants-2008_07 |
| ORD ID | ord-70b62e78ab69429c94b4d30757a4585a |
| 출처 메모 | uspto-grants-2008_07 |