Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Potassium Iodide → Methyl alpha-(4-chloro-5,6,7,8-tetrahydro-1-naphthyloxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Sodium Methoxide | HCID 10942334 | — |
| 반응물 | 4-Chloro-5,6,7,8-tetrahydronaphthalen-1-ol | HCID 20203333 | — |
| 반응물 | Methyl alpha-Bromo-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 20392594 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl alpha-(4-chloro-5,6,7,8-tetrahydro-1-naphthyloxy)-alpha-[p-(p-chlorophenoxy)phenyl]acetate | HCID 12531871 | — |
반응 단계
To a solution of 1.19 g of sodium methoxide, 4.57 g of 4-chloro-5,6,7,8-tetrahydro-1-naphthol, and 100 mg of potassium iodide was added 7.11 g of methyl α-bromo-α-[p-(p-chlorophenoxy)phenyl]acetate in 10 ml of benzene. The mixture was heated at reflux overnight, cooled to room temperature, and poured into 100 ml of water. The mixture was then extracted with 2×75 ml of ether. The combined extracts were washed with 2×50 ml of 5% NaOH, 2×50 ml of water, 50 ml of saturated brine, and dried (MgSO4). Evaporation of the solvent yielded an oil which was chromatographed over 100 g of silica gel (benzene). Concentration of cuts yielded a yellow gum which solidified on standing to give the product as a white solid, mp 87.5°-90° C. (6.4 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04168385 |
| 출처 데이터셋 | uspto-grants-1979_09 |
| ORD ID | ord-740e6d6ca3204dcc9b4ca04665a9ca90 |
| 출처 메모 | uspto-grants-1979_09 |