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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611886Generated: November 4, 2026

N,N-Dimethylaniline → 2,3-Dimethyl-5,12-dihydrobenzo[b]phenazine

https://huagongshe.com/reaction/1611886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantDichloromethaneHCID 6344—
Reactant2,3-DihydroxynaphthaleneHCID 7091—
Reactant4,5-Dimethyl-1,2-phenylenediamineHCID 76635—
SolventTolueneHCID 1140—
SolventHeptaneHCID 8900—
Product2,3-Dimethyl-5,12-dihydrobenzo[b]phenazineHCID 2225146933%

Reaction Steps

2,3-dihydroxynapthalene (10 g, 62.5 mmol), 4,5-dimethyl-1,2-phenylenediamine (8.5 g, 62.5 mmol) and N,N-dimethylaniline (54 ml) are placed into a round bottom flask under nitrogen atmosphere. Mixture is stirred at reflux. Reaction is monitored by TLC (CH2Cl2:Heptane/1:1) until all 2,3-dihydroxynaphthalene has reacted (˜3 hours). After cooling to room temperature, toluene (100 ml) is added and solid is collected by vacuum filtration. After washing with toluene (50 ml), ethanol (100 ml) and hexanes (50 ml), the product is dried under vacuum to yield 23.3 g (33% yield) of light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06991859B2
Source datasetuspto-grants-2006_01
ORD IDord-48ab1d27ec6348ac806381ca6969003f
Source noteuspto-grants-2006_01