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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38676생성일: 2026년 10월 24일

Iodine → ethyl 2-(3,5-dimethyl-1H-pyrazol-1-yl)propanoate

https://huagongshe.com/ko/reaction/38676

반응식

참여 물질

역할이름HCID투입량
반응물IodineHCID 807—
반응물3,5-DimethylpyrazoleHCID 6210—
반응물Potassium CarbonateHCID 11430—
반응물Ethyl 2-bromopropionateHCID 79040—
용매AcetonitrileHCID 6342—
생성물ethyl 2-(3,5-dimethyl-1H-pyrazol-1-yl)propanoateHCID 12008675—

반응 단계

A suspension of 3,5-dimethyl-1H-pyrazole (Aldrich, 8 g, 0.083 mol), anhydrous K2CO3 (11.50 g, 0.083 mol) and ethyl 2-bromopropanoate (Aldrich, 15 g, 0.083 mol) in 50 mL of dry ACN was refluxed with mechanical stirring for 24 h. Reaction was checked by TLC (iodine), and starting material was detected, so 0.2 equivalents of K2CO3 were added to the mixture which was refluxed over weekend. Reaction was checked, starting material was still detected. 0.2 eq. of K2CO3 were added to the mixture, which was refluxed during 24 h. Reaction was stopped, no advances were observed. Reaction mixture was filtered. Solvent was evaporated under reduced pressure. Residue was diluted with 50 ml of DCM, and washed with water. Organic layer was separated and aqueous fraction was extracted three times with 70 mL of DCM. Combined organic extracts were washed with brine, dried over Na2SO4 (anh), filtered and concentrated under reduce pressure. Residue was purified by chromatographic column 70 g cartridge (ISOLUTE silica) using Hex/EtOAc 100/0 to 20/80 giving (11.6 g 71%) colourless oil. 1H NMR (300 MHz, CDCl3) δ ppm: 5.83 (s, 1H), 4.85 (q, 1H), 4.08-4.25 (m, 2H), 2.22-2.23 (m, 6H), 1.79 (d, 3H), 1.23 (t, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524750B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-22c27cacdc74464198a9ab92f9f8da1e
출처 메모uspto-grants-2013_09