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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 530631Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/530631

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktNitromethaneHCID 6375—
Edukt1,1,3,3-TetramethylguanidineHCID 66460—
EduktEthyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
LösungsmittelWaterHCID 962—
ProduktEthyl 4,4,4-trifluoro-3-(nitromethyl)butanoateHCID 26836398%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09353096B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-20e0dafa53e34ec19e2e5b1d6463eff7
Quellennotizuspto-grants-2016_05