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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12827생성일: 2026년 10월 23일

Hydrochloric Acid → ethyl 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylate

https://huagongshe.com/ko/reaction/12827

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Tert-Butyl nitriteHCID 10906—
반응물ethyl 5-amino-1-(tert-butyl)-1H-pyrazole-4-carboxylateHCID 13809946—
용매AcetonitrileHCID 6342—
생성물ethyl 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylateHCID 1380994739%

반응 단계

To a mixture of t-butyl nitrite (7.2 mL, 60.5 mmol), cuprous chloride (4.8 g, 48.5 mmol), and anhydrous acetonitrile (120 mL) was added 5-amino-1-tert-butyl-1H-pyrazole-4-carboxylic acid ethyl ester (8.4 g, 39.8 mmol) in portions over 30 minutes at 0° C. The reaction mixture was stirred at room temperature for 1 h, then at 65° C. for 1 h. The mixture was then poured into 6N HCl (120 mL) and extracted with dichloromethane. The aqueous phase was extracted three times with dichloromethane. After the combined organic phases were concentrated in vacuo, the crude residue was purified by flash chromatography eluting with a gradient of 0-20% ethyl acetate/hexanes, then 20% ethyl acetate/hexanes to give 1-tert-butyl-5-chloro-1H-pyrazole-4-carboxylic acid ethyl ester (5.5 g, 39%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-04c1057d28d84cdc850db8b6d209f025
출처 메모uspto-grants-2010_06