돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 704813생성일: 2026년 10월 23일

p-Toluenesulfonic acid → (E)-1-[3-(4-Chlorophenoxy)phenyl]buten-3-one

https://huagongshe.com/ko/reaction/704813

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Sodium HydroxideHCID 14798—
반응물3-(4-Chlorophenoxy)benzaldehydeHCID 616015—
용매AcetoneHCID 180—
용매TolueneHCID 1140—
생성물(E)-1-[3-(4-Chlorophenoxy)phenyl]buten-3-oneHCID 20073366—

반응 단계

10 N aqu. NaOH (2 ml) was added to a solution of 3-(4-chlorophenoxy)-benzaldehyde (23.3 g, Aldrich) in acetone (150 ml) and stirred vigorously. After a few minutes' stirring, the temperature rose to 32° C. The mixture was left for 5 minutes and then poured into 2 M aqu. HCl (600 ml) and extracted with ether/pet. ether (1:1, 200 ml). The extract was washed with water and satd. aqu. NaCl, dried over MgSO4, and stripped to give the aldol product. The latter was taken up in toluene (300 ml), p-toluenesulphonic acid (1 g) was added, and the mixture heated for 1 hour. The mixture was then cooled, washed with satd. aqu. NaHCO3 and satd. aqu. NaCl, dried over MgSO4 and stripped. The residue was eluted through a slice gel column using methylene chloride/40-60 pet. ether (1:1, followed by 3:1) and the eluate stripped to give the desired product (19 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04988733
출처 데이터셋uspto-grants-1991_01
ORD IDord-b20afd6f017c485282cb258baae5a590
출처 메모uspto-grants-1991_01