Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 661846Erstellt: 27. Oktober 2026

Aniline → 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide

https://huagongshe.com/reaction/661846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAnilineHCID 6115—
EduktThionyl ChlorideHCID 24386—
Edukt3-Bromo-6-hydroxy-2-methylbenzoic acidHCID 11053451—
EduktHCID 178418385HCID 178418385—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt3-bromo-6-hydroxy-2-methyl-N-phenylbenzamideHCID 5937498868,4%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

Step 3 Thionyl chloride (0.111 mL, 1.524 mmol) was added to a solution of benzotriazole (594 mg, 4.99 mmol) in DCM (8 mL) at rt and the mixture was stirred for 30 min. A solution of 3-bromo-6-hydroxy-2-methylbenzoic acid (320 mg, 1.385 mmol) in THF (8.00 mL) was added and the mixture was stirred at rt for 2 hrs. The mixture was filtered and the solid was washed with DCM (3 mL). The filtrate was concentrated, and the residue was dissolved in aniline (2 g, 21.48 mmol) and heated in a sealed tube by microwave irradiation at 150° C. for 10 min. The mixture was diluted with EtOAc (100 mL) and washed with 2 M hydrochloric acid (20 mL), water (10 mL) and brine (10 mL), dried and concentrated. The residue was triturated with DCM (4 mL) to give the 3-bromo-6-hydroxy-2-methyl-N-phenylbenzamide as light-colored solid (290 mg, 68%). Mass spectrum m/z 306, 308 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084620B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-f4ced408da1d45c3b3fc541e7389ffb1
Quellennotizuspto-grants-2011_12