Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-tert-Butylbenzyl alcohol → 4-(4-t-Butylbenzyloxy)-5-methoxypyrimidine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-tert-Butylbenzyl alcohol | HCID 13416 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 4-Chloro-5-methoxypyrimidine | HCID 11008039 | — |
| 용매 | Dimethylacetamide | HCID 31374 | — |
| 생성물 | 4-(4-t-Butylbenzyloxy)-5-methoxypyrimidine | HCID 76853235 | 77% |
반응 단계
To a solution of 4-chloro-5-methoxypyrimidine (1.5 g, 10.3 mmol) described in Journal of the Chemical Society (1960), 4590, and 4-t-butylbenzylalcohol (2.55 g, 15.6 mmol) in dimethylacetamide (10 mL) was added sodium hydride (0.625 g, 15.6 mmol) at 0° C., and the mixture was stirred at room temperature for 3 hrs. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 4-(4-t-butylbenzyloxy)-5-methoxypyrimidine (2.16 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08895574B2 |
| 출처 데이터셋 | uspto-grants-2014_11 |
| ORD ID | ord-93733c3d90984d0eb0ecac29f21d3b54 |
| 출처 메모 | uspto-grants-2014_11 |