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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642637Generated: November 2, 2026

Sodium Carbonate → HCID 66756816, compound

https://huagongshe.com/reaction/1642637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Benzyloxy-4-bromomethyl-1-nitrobenzeneHCID 62115042—
Reactant2-methyl-6-(tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrileHCID 66757026—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 66756816HCID 66756816—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 2-benzyloxy-4-bromomethyl-1-nitrobenzene (2.99 g, 9.27 mmol) and Pd(PPh3)4 (536 mg, 0.464 mmol) in DME (10 mL) is heated to 60° C. for 2 min. in a microwave. 2-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzonitrile (5.96 g of crude, ˜13.9 mmol) in DME (10 mL) and EtOH (2 mL) is added along with Na2CO3 (2 M, 3.3 mL). The reaction mixture is heated to 110° C. for 30 min. by microwave. Then the reaction is heated to 120° C. for an additional 15 min. by microwave. The reaction mixture is diluted with DCM (150 mL) and extracted with water (50 mL). The aqueous layer is extracted with DCM (30 mL) and the combined organics is dried over Na2SO4. Evaporation yields a brown oil, and it is then purified by flash column to yield a tan solid as the title compound: MS (M−H)−=357.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119666B2
Source datasetuspto-grants-2012_02
ORD IDord-a533f2e851034182b7e3ffad2cf13a18
Source noteuspto-grants-2012_02