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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811026Generated: October 25, 2026

Aniline → HCID 59374988, compound

https://huagongshe.com/reaction/1811026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantThionyl ChlorideHCID 24386—
Reactant3-Bromo-6-hydroxy-2-methylbenzoic acidHCID 11053451—
ReactantHCID 178418385HCID 178418385—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 59374988HCID 5937498868.4%

Reaction Conditions

Temperature150 °C

Reaction Steps

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362065B2
Source datasetuspto-grants-2013_01
ORD IDord-fddee5f9c6364155b35cd980ff925283
Source noteuspto-grants-2013_01