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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12879생성일: 2026년 10월 23일

Hydrochloric Acid → 5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/12879

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Tert-Butyl nitriteHCID 10906—
반응물ethyl 5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylateHCID 351028—
촉매Cuprous chlorideHCID 62652—
용매AcetonitrileHCID 6342—
생성물5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl esterHCID 6702092642%

반응 단계

Copper(I) chloride (2.500 g, 25.25 mmol) was suspended in 7.0 mL cold (ice/acetone bath) anhydrous acetonitrile. t-Butyl nitrite (5.75 mL, 90%, 43.56 mmol) was added, followed by a suspension of 5-amino-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester (4.408 g, 18.58 mmol) in 27.0 mL acetonitrile. The mixture was stirred at room temperature for 45 minutes and then at 70° C. for 1.25 hour. The mixture was cooled to room temperature, slowly added to 6N HCl (17.5 mL) and then extracted with methylene chloride. The organic phase was washed sequentially with water and brine. The aqueous phases were back extracted with a second portion of methylene chloride. The two organic phases were combined, dried over sodium sulfate and concentrated in vacuo. The crude residue was chromatographed by flash chromatography eluting with a gradient of 10-50% ethyl acetate/hexanes to give 5-chloro-1-cyclohexyl-1H-pyrazole-4-carboxylic acid ethyl ester (1.98 g; 42%). Mass spectrum: m/z: 257.3 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728029B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b3919ed3436a4960839e99ad25df6759
출처 메모uspto-grants-2010_06