Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410606Generated: November 2, 2026

1,2-Dichloroethane → HCID 66677471, compound

https://huagongshe.com/reaction/2410606

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2-(Methoxymethyl)-2'-methylbiphenyl-4-carboxylic acidHCID 59495822—
ReactantHCID 76685353HCID 76685353—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
ProductHCID 66677471HCID 66677471—

Reaction Steps

To a solution of Intermediate 75 (0.270 g, 0.83 mmol) and Intermediate 3 (0.192 g, 0.75 mmol) in ACN (2 mL) was added EDC (0.201 g, 1.05 mmol). The reaction mixture was stirred at room temperature for 18 hours. The reaction mixture was diluted with pyridine (2 mL) and heated at 150° C. under microwave irradiations for 45 minutes. The solvent was removed in vacuo and the residue dissolved in DCM. The mixture was washed with water and the organic phase passed through a hydrophobic frit. The solvent was evaporated in vacuo. The residue was purified by flash chromatography (silica, iso-hexane/EtOAc) to afford the title compound. 1H NMR (CDCl3, 400 MHz) δ 8.43 (1H, d, J=1.8 Hz), 8.21 (1H, d, J=1.7 Hz), 8.17 (1H, dd, J=7.9, 1.9 Hz), 8.08 (1H, dd, J=8.0, 1.7 Hz), 7.72 (1H, d, J=8.0 Hz), 7.35-7.21 (4H, m), 7.13 (1H, d, J=7.4 Hz), 4.29-4.17 (2H, m), 3.90 (2H, s), 3.33 (3H, s), 3.29 (2H, s), 2.46 (3H, s), 2.08 (3H, s), 1.50 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815919B2
Source datasetuspto-grants-2014_08
ORD IDord-611d2e199d9543659381c6ff2b7b777a
Source noteuspto-grants-2014_08