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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 469311Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/469311

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktThionyl ChlorideHCID 24386—
EduktBromineHCID 24408—
EduktChlorineHCID 24526—
Edukt2-Bromoisonicotinic acidHCID 222701—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt4-Methyl-3H-benzooxazol-2-oneHCID 12709336—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-(2-bromo-pyridine-4-carbonyl)-4-methyl-3H-benzoxazol-2-oneHCID 58181213—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08629137B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-a7869bb0c12f4d85aef225774e98f332
Quellennotizuspto-grants-2014_01