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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469311Generated: October 26, 2026

Dimethylformamide → 6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-one

https://huagongshe.com/reaction/469311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
ReactantBromineHCID 24408—
ReactantChlorineHCID 24526—
Reactant2-Bromoisonicotinic acidHCID 222701—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant4-Methyl-3H-benzooxazol-2-oneHCID 12709336—
SolventDichloromethaneHCID 6344—
Product6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181213—

Reaction Conditions

Temperature130 °C

Reaction Steps

2.20 mL (30.0 mmol) thionyl chloride and 0.390 mL (4.80 mmol) DMF were added to 2.00 g (9.90 mmol) 2-bromopyridine-4-carboxylic acid in 30 mL DCM and refluxed for 2 h. The reaction mixture was evaporated to dryness and coevaporated twice with toluene. The residue was combined with 6.24 g (46.8 mmol) aluminium trichloride and 1.50 g (10.1 mmol) 4-methyl-3H-benzoxazol-2-one and the mixture obtained was stirred overnight at 110° C. and for 5 hours at 130° C. The mixture was decomposed with ice water and extracted twice with DCM. The organic phases were dried on magnesium sulphate, filtered and evaporated down i. vac. The residue was triturated with DIPE/MeOH and suction filtered. The product obtained is a mixture of the corresponding bromine and chlorine compound (40/60).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-a7869bb0c12f4d85aef225774e98f332
Source noteuspto-grants-2014_01