Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62718Generated: October 30, 2026

Triethylamine → HCID 67041561, compound

https://huagongshe.com/reaction/62718

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3,5-Dibromo-4-ethoxyanilineHCID 43351697—
Reactant4-(3,5-Dichloro-4-hydroxyphenylcarbamoyl)benzoic acidHCID 67041895—
SolventDichloromethaneHCID 6344—
ProductHCID 67041561HCID 6704156191%

Reaction Steps

3,5-Dibromo-4-ethoxyaniline (2) (100 mg, 339 μmol) was dissolved in DCM (2.5 mL) and treated with triethylamine (143 μL, 1.02 mmol). 4-(Chlorocarbonyl)benzoic acid methyl ester (3) (135 mg, 678 μmol) was added in one portion and the resultant dark orange mixture was stirred at RT for 3 h then partitioned between EtOAc and aqueous 1M HCl. The organic layer was washed successively with saturated aqueous NaHCO3, water and brine. The organic layer was then dried over MgSO4, filtered and the solvent evaporated in vacuo. The residue was triturated from Et2O and filtered. The filtered solid was washed with methanol and the washings were concentrated in vacuo to provide methyl 4-(3,5-dibromo-4-ethoxyphenylcarbamoyl)benzoate (4) (141 mg, 73%) as a pale brown solid: m/z 456 [M−H]− (ES−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447028B2
Source datasetuspto-grants-2016_09
ORD IDord-29f88504e4be420283fd0b5c412dddbb
Source noteuspto-grants-2016_09