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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 599312생성일: 2026년 10월 26일

Carbon Dioxide → 1-tert-Butyl-1H-pyrazole-4-carboxylic acid

https://huagongshe.com/reaction/599312

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물4-Bromo-1-(1,1-dimethylethyl)-1H-pyrazoleHCID 53216898—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물1-tert-Butyl-1H-pyrazole-4-carboxylic acidHCID 2469629167%

반응 조건

온도-78 °C

반응 단계

To a −78° C. solution of 4-bromo-1-t-butyl-1H-pyrazole (15 g, 74.3 mmol) in anhydrous THF (100 mL) was added n-BuLi (2.5 M in hexane, 53 mL, 132 mmol) under N2, and the resulting mixture was stirred at −78° C. for 30 min. Excess dry ice was added at −78° C., and the mixture was warmed slowly to RT and stirred overnight. The reaction was concentrated in vacuo, water was added and the pH was adjusted to pH 3 by the addition of 2N aq HCl. The aqueous solution was extracted with EtOAc. The extracts were washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was recrystallized (EtOAc-pet. ether) to give 1-t-butyl-1H-pyrazole-4-carboxylic acid (8.0 g, 67% yield). 1H NMR (300 MHz, CDCl3): δ 8.10 (s, 1 H), 8.03 (s, 1 H), 1.64 (s, 9 H); MS (ESI) m/z: 168.9 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897762B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-37b8b203c16841d38f21c12262051204
출처 메모uspto-grants-2011_03