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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266204Generated: October 30, 2026

Triethylamine → HCID 54067980, compound

https://huagongshe.com/reaction/266204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 10805061HCID 10805061—
CatalystDimethylformamideHCID 6228—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 54067980HCID 540679809%

Reaction Steps

A solution of 3'-cyclopentyloxy-4'-methoxy-biphenyl-4-carboxylic acid (0.5 g, 1.602 mmol) in toluene (30 mL) was treated with a 2M solution of oxalyl chloride (0.840 mL, 1.68 mmol) in dichloromethane and 1 drop of dimethyl formamide was added. This mixture was heated to reflux for ten minutes, cooled and concentrated in vacuo to an oil. This oil is dissolved in dichloromethane and added dropwise to a mixture of hydroxylamine hydrochloride (0.139 g, 1.25 eq) and triethylamine (0.405 g, 2.5 eq) in dichloromethane (10 mL). After about thirty minutes the reaction the reaction appears to go no further, some of the starting acid remains (by tlc). The reaction is washed with water dried and concentrated. The material is purified via reversed phase HPLC, using a Dynamax-60A Phenyl column wand 70% acetonitrile/water as carrier. This provided the title compound in 9% yield as a crystalline solid (CH2Cl2). mp 181°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650444
Source datasetuspto-grants-1997_07
ORD IDord-cdf60409c7ac469cb88ecd83b0884a21
Source noteuspto-grants-1997_07