Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536617Generated: October 29, 2026

Sodium Carbonate → HCID 67254694, compound

https://huagongshe.com/reaction/536617

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,4-DibromothiopheneHCID 18452—
Reactant3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 56776929—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
SolventEthanol toluene waterHCID 86587398—
ProductHCID 67254694HCID 6725469469%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3,4-dibromothiophene (3 g, 12.5 mmol), 3-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (2 g, 12.5 mmol), Na2CO3 (2.7 g, 25 mmol), Pd(PPh3)4 (1.4 g, 1.25 mmol) in a mixture of toluene/EtOH/H2O (40 mL, 5:3:2) was stirred at 80° C. under nitrogen overnight. The reaction mixture was diluted with EtOAc (80 mL), and washed with water and brine. The organic phase was dried over Na2SO4, concentrated in vacuo, and purified on silica gel column (PE: EtOAc=30:1) to afford 4-(4-bromothiophen-3-yl)-3-methylbenzonitrile (Scheme III, 13, X1=4-cyano-2-methylphenyl) (2.4 g, yield 68%) as yellow oil. 1H NMR (CD3OD 400 MHz): δ 7.56 (s, 1H), 7.50-7.48 (m, 2H), 7.31 (d, J=3.2 Hz, 1H), 7.22 (d, J=7.6 Hz, 1H), 2.10 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859611B2
Source datasetuspto-grants-2014_10
ORD IDord-3eacde70836241928a06b88412f43348
Source noteuspto-grants-2014_10