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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 530631생성일: 2026년 10월 26일

Sulfuric Acid → Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoate

https://huagongshe.com/reaction/530631

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물NitromethaneHCID 6375—
반응물1,1,3,3-TetramethylguanidineHCID 66460—
반응물Ethyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
용매WaterHCID 962—
생성물Ethyl 4,4,4-trifluoro-3-(nitromethyl)butanoateHCID 26836398%

반응 단계

A mixture of 4.203 g (25 mmol) of ethyl 4,4,4-trifluoro-crotonate, 20 mL of nitromethane and ca. 0.576 g (5 mmol) of tetramethyl guanidine was stirred for 13 h at room temperature, and then diluted with water and acidified by the addition of 0.5 M sulfuric acid. The mixture was extracted three times with diethyl ether. The combined ether extracts were washed with water, and then brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. to give 5.601 g (98%) of 4,4,4-trifluoro-3-nitromethyl-butyric acid ethyl ester as an amber oil. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.21 (t, J=7.15 Hz, 3H) 2.76 (dd, J=6.53, 1.76 Hz, 2H) 3.61-3.84 (m, 1H) 4.13 (q, J=7.11 Hz, 2H) 4.83-5.01 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09353096B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-20e0dafa53e34ec19e2e5b1d6463eff7
출처 메모uspto-grants-2016_05