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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467552Generated: October 30, 2026

1,2-Dichloroethane → HCID 59002672, compound

https://huagongshe.com/reaction/467552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAcetic AcidHCID 176—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 58992419HCID 58992419—
SolventDichloromethaneHCID 6344—
ProductHCID 59002672HCID 59002672—

Reaction Steps

Into an 8 ml sealed tube, was placed acetic acid (48 mg, 0.80 mmol). This was followed by the addition of a solution of 2′-Methyl-5′-oxazol-2-yl-biphenyl-4-ylamine (100 mg, 0.40 mmol) in CH2Cl2 (2 g) with stirring for 10 mins in a bath of H2O/ice. This was followed by the addition of a solution of EDC (90 mg, 0.47 mmol) in CH2Cl2 (2 g). The resulting solution was allowed to react, with stirring, overnight while the temperature was maintained at room temperature. The reaction progress was monitored by TLC (EtOAc/PE=1:1). The resulting mixture washed 3 times with 10 ml of HCl(10%), 3 times with 10 ml of sat.NaHCO3 and 3 times with 10 ml of H2O. The organic layer was dried over Na2SO4. Removal of the solvents under reduced pressure afforded the title compound, N-(2′-Methyl-5′-oxazol-2-yl-biphenyl-4-yl)-acetamide, as a yellow solid (82 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623871B2
Source datasetuspto-grants-2014_01
ORD IDord-13f1967e5d314fc38bbb1260bf56c0c8
Source noteuspto-grants-2014_01