HomeMCPWorkbenchSkills
HomeWorkbenchNotificationsMe
llms.txt · MCP GuidePrivacy Policy · Terms of Service · Supportv1.8.0
  1. Home
  2. /Reaction

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

HRID 895965
Notes
Print preview

Reaction equation

HRID 895965 reaction equation
O[C:2]1[C:11](O)=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=1.[CH3:13][C:14]1[C:19]([CH3:20])=[CH:18][C:17]([NH2:21])=[C:16]([NH2:22])[CH:15]=1.CN(C)C1C=CC=CC=1.C(Cl)Cl>C1(C)C=CC=CC=1.CCCCCCC>[CH3:13][C:14]1[C:19]([CH3:20])=[CH:18][C:17]2[NH:21][C:2]3[CH:3]=[C:4]4[CH:5]=[CH:6][CH:7]=[CH:8][C:9]4=[CH:10][C:11]=3[NH:22][C:16]=2[CH:15]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 949N,N-DimethylanilineHCID 6344DichloromethaneHCID 70912,3-Dihydroxynaphthalene2×HCID 766354,5-Dimethyl-1,2-phenylenediamine

Product 1

HCID 222514692,3-Dimethyl-5,12-dihydrobenzo[b]phenazineYield 33%

Reagents, catalysts & solvents 2

HCID 1140
Toluene
Solvent
HCID 8900HeptaneSolvent

Procedure

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.

Workup

  1. temperatureat reflux
  2. customReaction
  3. customhas reacted (˜3 hours)
  4. filtrationsolid is collected by vacuum filtration
  5. washAfter washing with toluene (50 ml), ethanol (100 ml) and hexanes (50 ml)
  6. customthe product is dried under vacuum
  7. customto yield 23.3 g (33% yield) of light yellow solid

Sources & evidence

ORD record
ord-503236e280544a02887307e48aefe752
Source dataset
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06919140B2

Reaction notes

Loading…

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes