Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Ethyl-6-methylphenol → 4-Bromo-2-ethyl-6-methylphenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Ethyl-6-methylphenol | HCID 519333 | — |
| 반응물 | Tetra-n-butylammonium tribromide | HCID 23500184 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 4-Bromo-2-ethyl-6-methylphenol | HCID 22006838 | 182.7% |
반응 단계
Then, 16 g of 2-ethyl-6-methylphenol was dissolved in 200 ml of chloroform, followed by stirring at 0° C., to which 56.6 g of tetrabutylammonium tribromide was added in small portions. After stirring at room temperature for 1 hour, the solvent was removed by distillation under reduced pressure, and the residue was dissolved in 300 ml of diethyl ether. The solution was successively washed with 10% hydrochloric acid and water, dried with anhydrous magnesium sulfate, and concentrated to obtain a crude product. The crude product was subjected to silica gel chromatography, which afforded 23 g of 4-bromo-2-ethyl-6-methylphenol (92% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05872137 |
| 출처 데이터셋 | uspto-grants-1999_02 |
| ORD ID | ord-12b1d64a1dd3461ba4f2a029abab3055 |
| 출처 메모 | uspto-grants-1999_02 |