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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611491생성일: 2026년 10월 26일

Nitric Acid → 4-(5-Nitro-thiophen-2-yl)-butyric acid methyl ester

https://huagongshe.com/reaction/1611491

반응식

참여 물질

역할이름HCID투입량
반응물Nitric AcidHCID 944—
반응물4-(2-Thienyl)butanoic acid methyl esterHCID 140766—
용매Acetic AnhydrideHCID 7918—
생성물4-(5-Nitro-thiophen-2-yl)-butyric acid methyl esterHCID 69233400—

반응 단계

To 8 mL of acetic anhydride at −20° C. is added 1.2 mL of nitric acid (d=1.5). The mixture is kept at −20° C., and a solution of 4-thiophen-2-yl-butyric acid methyl ester (1.84 g, 10.0 mmol) in 12 mL of acetic anhydride is added dropwise. The reaction mixture is stirred for 10 minutes after completion of addition, and poured into an ice-water mixture. The product is extracted with ethyl acetate and the organic layer is washed with 10 N aqueous sodium hydroxide solution, dried and concentrated. The residue is purified by flash column chromatography eluting with 1:4 ethyl acetate:hexane to provide 1.32 g of 4-(5-nitro-thiophen-2-yl)-butyric acid methyl ester as a yellow oil; 1H NMR (DMSO-d6) δ 1.93 (quintet, J=7 Hz, 2H), 2.41 (t, J=7 Hz, 2H), 2.88 (t, J=7 Hz, 2H), 3.59 (s, 3H), 7.04 (d, J=5 Hz, 1H), 8.01 (d, J=5 Hz, 1H); MS 229.0 (M)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06987116B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-428f1f5596d141b0bd4ef094d4044da1
출처 메모uspto-grants-2006_01