돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2164644생성일: 2026년 10월 26일

Chloroacetonitrile → (4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrile

https://huagongshe.com/reaction/2164644

반응식

참여 물질

역할이름HCID투입량
반응물ChloroacetonitrileHCID 7856—
반응물Potassium CarbonateHCID 11430—
반응물Sodium HydroxideHCID 14798—
반응물Phenol, 4-(4-(methylsulfonyl)phenoxy)-HCID 514882—
용매AcetonitrileHCID 6342—
생성물(4-(4-(Methylsulfonyl)phenoxy)phenoxy)acetonitrileHCID 1307852092.4%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04505929
출처 데이터셋uspto-grants-1985_03
ORD IDord-36a243dff25145769df82ed4d451001c
출처 메모uspto-grants-1985_03