Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2177363Generated: November 1, 2026

Dimethylformamide → HCID 90418142, compound

https://huagongshe.com/reaction/2177363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl cyanoacetateHCID 7764—
ReactantHCID 90418133HCID 90418133—
SolventEthyl AcetateHCID 8857—
ProductHCID 90418142HCID 90418142—

Reaction Conditions

Temperature0 °C

Reaction Steps

Into a 100-mL round-bottom flask, was placed 3-(acetylsulfanyl)-1,1,1-trifluorobutan-2-one (5.8 g, 28.97 mmol, 1.00 equiv), N,N-dimethylformamide (10 mL). This was followed by the addition of TEA (3 g, 29.65 mmol, 1.02 equiv) and ethyl 2-cyanoacetate (3.27 g, 28.91 mmol, 1.00 equiv) dropwise with stirring at 0° C. The resulting solution was stirred overnight at 25° C. Then it was diluted with 20 mL of EA. The organic phase was separated and washed with 3×20 mL of H2O. The mixture was dried over anhydrous sodium sulfate. The solids were filtered out. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (30/70). The collected fractions were combined and concentrated under vacuum. This resulted in 6.5 g (79%) of ethyl 2-amino-4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiophene-3-carboxylate as a dark red liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067898B1
Source datasetuspto-grants-2015_06
ORD IDord-d560489600754cf3a547f75d413d57cd
Source noteuspto-grants-2015_06