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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992797Generated: October 30, 2026

1,2-Dichloroethane → HCID 86761041, compound

https://huagongshe.com/reaction/1992797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
ReactantHOAtHCID 181649—
Reactant4-(Trifluoromethoxy)anilineHCID 600848—
ReactantHCID 68428139HCID 68428139—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 86761041HCID 86761041—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of the intermediate from step D (0.1 g, 0.41 mmol) in DMF (2 mL) was added 4-trifluoromethoxy aniline (83 μL, 0.61 mmol), DIEA (215 μL, 1.23 mmol), HOAt (0.08 g, 0.61 mmol) and EDC (0.118 g, 0.61 mmol). The reaction was heated at 50° C. for 3 hours. The reaction was diluted with ethyl acetate, washed with 1N HCl , saturated NaHCO3, and saturated NaCl solutions. The organic layer was dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography using 30% ethyl acetate hexanes. 1H NMR (DMSO, 500 MHz): 10.34 (bs, 1H), 7.93 (d, J=5.9 Hz, 2H), 7.8 (bm, 2H), 7.44 (bs, 1H), 7.37 (bd, J=8.0 Hz, 2H). LC-MS=3.76 min; (M+H)=402.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07649009B2
Source datasetuspto-grants-2010_01
ORD IDord-01ded6e49f1047839ba094d839d771ac
Source noteuspto-grants-2010_01