Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850093Generated: November 2, 2026

Dichloromethane → HCID 67343116, compound

https://huagongshe.com/reaction/1850093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Tolylboronic acidHCID 2733950—
ReactantHCID 87364079HCID 87364079—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67343116HCID 6734311672.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To the title compound of Step A (0.12 g, 0.27 mmol), 3-methylphenylboronic acid (0.08 g, 0.60 mmol), K3PO4 (0.128 g, 0.54 mmol), Pd(dppf)Cl2.CH2Cl2 (0.013 g, 0.017 mmol) and dppf (0.006 g, 0.010 mmol) was added dioxane (3 mL). The flask was heated at 100° C. for 18 h, cooled to rt, diluted with EtOAc and filtered through a small silica pad. Silica gel chromatography (10-40% EtOAc in hexanes) gave 0.073 g (72% yield) of the title compound. 1H NMR (CDCl3): 7.31-7.26 (m, 4H), 7.18-7.15 (m, 1H), 7.05 (dd, J=8.2, 2.0 Hz, 1H), 6.57 (d, J=1.9 Hz, 1H), 4.86-4.81 (m, 1H), 4.30-4.26 (m, 2H), 3.96 (dd, J=10.2, 4.2 Hz, 2H), 2.40 (s, 3H), 1.44 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957059B2
Source datasetuspto-grants-2015_02
ORD IDord-84b341b51b7f4f9fa95b7c28992a5b00
Source noteuspto-grants-2015_02