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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 432674생성일: 2026년 10월 26일

Citric Acid → 5-Formylthiophene-2-Carbonitrile

https://huagongshe.com/reaction/432674

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물DiisopropylamineHCID 7912—
반응물2-ThiophenecarbonitrileHCID 66087—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-Formylthiophene-2-CarbonitrileHCID 1228000455.3%

반응 단계

A solution of diisopropylamine (35.3 ml, 0.251 moles) in tetrahydrofuran (500 ml) was cooled to −78° C. under a nitrogen blanket. To this was added 1.6M n-butyllithium in hexanes (157 ml, 0.251 moles) and allowed to stir for 5 min. Then slowly added thiopene-2-carbonitrile (21.33 ml, 0.229 moles) in tetrahydrofuran (115 ml) and allowed to stir. After 45 min. was added NN-dimethylformamide (88.66 ml, 1.145 moles) at −78° C. Citric acid (40 g) was added after 2 h. followed by water (240 ml) and stirred for 18 h. The reaction was concentrated in vacuo, transferred to a separatory funnel, diluted with brine, and extracted twice with ether. The combined ether layers were washed with brine, dried over magnesium sulfate, filtered, and the solvent removed in vacuo. Chromatography yielded 15.8 g (50%) of 2-cyano-5-formylthiophene (EX-55A) as a brown solid: 1H NMR (300 MHZ, CDCl3) d 10.02 (s, 1H), 7.79 (m, 1H), 7.30 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06664255B1
출처 데이터셋uspto-grants-2003_12
ORD IDord-a63caca2447a4727828166c5acef299b
출처 메모uspto-grants-2003_12