Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chloroacetonitrile → (4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chloroacetonitrile | HCID 7856 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Phenol, 4-(4-(methylsulfonyl)phenoxy)- | HCID 514882 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrile | HCID 13078520 | 92.4% |
반응 단계
To a solution of 5.29 g (0.0200 mole) of 4-(4-(methylsulfonyl)phenoxy)phenol and 1.51 g (0.0200 mole) of 2-chloroacetonitrile in 100 ml of acetonitrile was added 3.0 g (0.0220 mole) of K2CO3. The mixture was heated at reflux for 3.5 hrs and cooled. The mixture was poured into aqueous NaOH and the product extracted from the mixture with CH2Cl2. The organic layer was extracted with aqueous NaOH, water and dried (Na2SO4). Removal of solvent in vacuo afforded 5.6 g (92.4% yield) of product. Recrystallization from ethanol followed by washing with aqueous NaOH and water afforded purified (4-(4-(methylsulfonyl)phenoxy)phenoxy)acetonitrile, mp 114°-115.5° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04505929 |
| 출처 데이터셋 | uspto-grants-1985_03 |
| ORD ID | ord-36a243dff25145769df82ed4d451001c |
| 출처 메모 | uspto-grants-1985_03 |