돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2183545생성일: 2026년 10월 25일

Acetic Acid → 4-(2,4,6-Trimethyl-phenyl)-2H-pyrazol-3-ylamine

https://huagongshe.com/reaction/2183545

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Hydrochloric AcidHCID 313—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물3-Oxo-2-(2,4,6-trimethyl-phenyl)-propionitrileHCID 22474397—
용매BenzeneHCID 241—
용매WaterHCID 962—
생성물4-(2,4,6-Trimethyl-phenyl)-2H-pyrazol-3-ylamineHCID 2247438610.3%

반응 단계

A mixture of 3-oxo-2-(2,4,6-trimethyl-phenyl)-propionitrile (2.300 g, 12.3 mmol), hydrazine hydrate (0.93 g) and glacial acetic acid (1.55 ml) in 20 ml benzene was heated at reflux for 4.5 hours. Reaction mixture was cooled to room temperature and 50 ml of 18.5% HCl in water was added. The benzene layer was separated and reextracted with 18.5% HCl. The aqueous layer were combined and neutralized with ammonium hydroxide and stirred at rt. overnight. Precipitate formed and was filtered to yield the title compound (0.256 g) as a yellow solid. The benzene layer was concentrated and purified through silica gel column using 5% methanol in chloroform as eluent to give an additional 1.450 g of the title compound; 1H NMR (CDCl3) ä 7.24(s, 1H), 6.95(s, 2H), 4.75(brs, 2H), 2.32(s, 3H), 2.13(s, 6H) ppm.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06900217B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-9b402513c4384f52b727e614cf322e46
출처 메모uspto-grants-2005_05