Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983802Generated: October 25, 2026

Triethylamine → 2-Hydroxy-N-methoxy-N-methyl-[1,1'-biphenyl]-3-carboxamide

https://huagongshe.com/reaction/983802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Phenylsalicylic acidHCID 9348—
ReactantOxalyl chlorideHCID 65578—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-Hydroxy-N-methoxy-N-methyl-[1,1'-biphenyl]-3-carboxamideHCID 1105431030.3%

Reaction Steps

2-hydroxy-3-phenylbenzoic acid (218, 3.0 g, 14 mmol) is dissolved in EtOAc (50 ml) and a few drops of DMF are added. Oxalyl chloride (2.5 ml, 1.5 eq) is added and the reaction is stirred under a dry atmosphere for 1 h. The reaction mixture is then concentrated in vacuo to yield a mixture of clear oil and white solid. This mixture is diluted with CH2Cl2 (50 ml) followed by the addition of N,O-dimethyl hydroxylamine hydrochloride (1.5 g, 1.1 eq) and triethylamine (3.9 ml, 2 eq). This mixture is stirred for 12-18 h under a dry atmosphere. Dilution of the reaction mixture with EtOAc and subsequent washing with dilute HCl and brine, followed by drying (MgSO4) and concentration in vacuo yields a mixture of reaction products. Flash chromatography (20/80 EtOAc/Hexanes) afforded N-methoxy-N-methyl-2-hydroxy-3-phenylbenzamide (219, 1.09 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867200B1
Source datasetuspto-grants-2005_03
ORD IDord-f276e7c9ffd34ec0ada420ba79622291
Source noteuspto-grants-2005_03