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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1017808Generated: October 26, 2026

Triethylamine → Benzanilide

https://huagongshe.com/reaction/1017808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantBenzyl p-aminobenzoateHCID 98488—
Reactant1,4-Benzenedicarboxylic acid, methyl esterHCID 3614454—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductBenzanilideHCID 7168134.8%

Reaction Steps

A solution of mono-methyl terephthalate (4.00 g, 22 mmol) in ethyl acetate (25 mL) and DMF (0.1 mL) was cooled in an ice bath and treated with oxalyl chloride (11 mL, 2N in CH2Cl2, 22 mmol) over 30 minutes. After stirring 2 hours at room temperature the solvent was removed on a rotary evaporator and the residue dissolved in CH2Cl2 (20 mL) and added to a solution of benzyl 4-aminobenzoate (5.00 g, 22 mmol) in CH2Cl2 (25 mL) and triethylamine (4.3 mL, 31 mmol) at −60° C. The reaction mixture was warmed to room temperature for 1 hour and then partitioned between water and ethyl acetate. The ethyl acetate layer was dried over sodium sulfate, filtered, and evaporated. The residue was recrystallized from t-butyl methyl ether to give 5.85 g of compound 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06479548B2
Source datasetuspto-grants-2002_11
ORD IDord-9f8d21a2aa104ff597679c335e1f7e44
Source noteuspto-grants-2002_11