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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243346Generated: October 27, 2026

O-Phenylenediamine → Diisopropyl Ether

https://huagongshe.com/reaction/2243346

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-PhenylenediamineHCID 7243—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductDiisopropyl EtherHCID 7914—
Product(2-Aminophenyl)amideHCID 86621027—

Reaction Steps

In a 50 ml three-necked flask, place 1.615 g of 7-nitro-9-oxo-9H-fluorene-4-carboxylic acid, which can be obtained according to WO2003057145, in suspension in 30 ml of dichloromethane, and then add successively 567 μl of oxalyl chloride and 1 drop of dimethylformamide. After stirring for 4 hours at room temperature, add 0.779 g of 1,2-diaminobenzene and 1.686 ml of triethylamine. After stirring for 20 hours at room temperature, the precipitate that formed is filtered off, and washed with water, then with a 10% saturated aqueous solution of sodium hydrogen carbonate and, finally, with water. After formation of a paste with diisopropyl ether, in this way we obtain 1.6 g of (2-aminophenyl)amide of 7-nitro-9-oxo-9H-fluoren -4-carboxylic acid, in the form of an orange powder, which is used as it is in the following stage, with the following characteristics:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674795B2
Source datasetuspto-grants-2010_03
ORD IDord-93653d4e4a06467ba82a12457e560c33
Source noteuspto-grants-2010_03