돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 345768생성일: 2026년 10월 24일

Pyridine → 2,3,6-trimethyl-4-(1H-pyrazol-5-ylimino)cyclohexa-2,5-dien-1-one

https://huagongshe.com/ko/reaction/345768

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl-HCID 70291—
반응물HCID 178418806HCID 178418806—
촉매Titanium TetrachlorideHCID 24193—
용매1,1-DichloroethaneHCID 6365—
생성물2,3,6-trimethyl-4-(1H-pyrazol-5-ylimino)cyclohexa-2,5-dien-1-oneHCID 17842825524.2%

반응 단계

A 1.62 ml quantity of pyridine was dissolved in 60 ml of dichloroethane, and 0.55 ml of titanium tetrachloride was added thereto. The mixture was refluxed with heating for 15 minutes. Then, to the mixture were added 1.50 g of 2,3,5-trimethyl-1,4-benzoquinone and 0.83 g of 3-aminopyrazole, and the mixture was refluxed with heating for 2 hours. The reaction mixture was cooled to room temperature and filtered through a Celite pad and the insoluble materials were washed there with chloroform. The filtrate was concentrated, and the resulting crude product was purified by silica gel column chromatography (eluent: diethyl ether-hexane=1:1), giving 0.52 g of 2,3,6-trimethyl-4-(3-pyrazolylimino)-2,5-cyclohexadien-1-one (Compound 37a) as a yellow solid. Table 3 below shows the structure and properties of Compound 37a.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05059598
출처 데이터셋uspto-grants-1991_10
ORD IDord-f8f076ed8eef4525bfae4655b36c182a
출처 메모uspto-grants-1991_10