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HRID 221860생성일: 2026년 10월 26일

Acetic Acid → 4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acid

https://huagongshe.com/reaction/221860

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물4-Hydrazinobenzoic acidHCID 12089—
반응물Pentanenitrile, 4,4-dimethyl-3-oxo-HCID 108871—
용매Tetrahydrofuran ethanolHCID 21873804—
생성물4-(5-Amino-3-tert-butyl-pyrazol-1-yl)-benzoic acidHCID 97468899%

반응 단계

A mixture of 4,4-dimethyl-3-oxo-pentanenitrile (4.52 g, 36.15 mmol), 4-hydrazinobenzoic acid (5.00 g, 32.86 mmol), and acetic acid (2 mL) in EtOH/THF (1:1) was refluxed for 16 h. After cooling, the solvent was concentrated at reduced pressure, and the crude was re-dissolved in EtOAc. The organic layer was washed with aqueous saturated Na2CO3 solution and brine, dried over MgSO4, filtered, and concentrated to half its volume. The resulting residue was filtered, and the solids were washed with cold EtOAc and dried under high vacuum to afford the title compound as a white solid (8.4 g, 99%). 1H-NMR (DMSO-d6) δ 12.91 (s, 1H), 7.99 (d, J=6.0 Hz, 2H), 7.75 (d, J=9.0 Hz, 2H), 5.42 (s, 1H), 5.39 (s, 2H), 1.21 (s, 9H); MS LC-MS [M+H]+=260, RT=1.83 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08207166B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-61257910ddf04c16842a9415e8734b1b
출처 메모uspto-grants-2012_06