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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1867507Generated: November 1, 2026

Sodium Carbonate → (2Benzo[1,2,5]oxadiazol-5-yl-phenyl)-dimethyl-amine

https://huagongshe.com/reaction/1867507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-N,N-dimethylanilineHCID 136527—
ReactantPotassium AcetateHCID 517044—
Reactant5-Bromo-2,1,3-benzoxadiazoleHCID 2776298—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product(2Benzo[1,2,5]oxadiazol-5-yl-phenyl)-dimethyl-amineHCID 68878349—

Reaction Conditions

Temperature80 °C

Reaction Steps

523 mg (1.65 eq.) bis(pinacolato)diboran, 552 mg (4.5 eq.) potassium acetate and 51 mg (0.01 eq.) PdCl(dppf)-CH2Cl2 are added to a solution of 373 mg 5-bromo-benzo[1,2,5]oxadiazole in 8 mL DMF and heated to 80° C. under continuous stirring for 6 hours. 662 mg (5 eq.) sodium carbonate in 3.3 mL water are added together with 500 mg (1 eq.) 2-bromo-N,N-dimethylaniline and 51 mg (0.01 eq.) PdCl(dppf)-CH2Cl2 to the reaction mixture, which is stirred for another 18 hours at 80° C., cooled to room temperature and extracted with ethyl acetate and water. The combined organic phases are washed with brine, dried over magnesium sulfate and evaporated. The residue is column chromatographed (hexane, then hexane/ethyl acetate 8:1) to yield the desired product as an orange resin. MS(ES+): 240 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07632851B2
Source datasetuspto-grants-2009_12
ORD IDord-84c49cd67ec942568ab3dc4c0b137042
Source noteuspto-grants-2009_12