Acetic Anhydride → HCID 18404845, compound
Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[NH:8][C:9]1[CH:14]=[CH:13][C:12]([Br:15])=[CH:11][C:10]=1[CH3:16].[C:17](OC(=O)C)(=O)[CH3:18]>C(O)(=O)C>[Br:15][C:12]1[CH:13]=[CH:14][C:9]([N:8]2[C:3]3[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=3[N:1]=[C:17]2[CH3:18])=[C:10]([CH3:16])[CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 5.22 g (18.8 mmol) of N-(2-aminophenyl)-4-bromo-2-methyl-aniline and 7.1 ml (75.2 mmol) of acetic acid anhydride is heated to boiling for 30 hours, combined with 15 ml of glacial acetic acid and heated to boiling for another 30 hours. Then the reaction mixture is concentrated and purified by flash chromatography (silica gel; methylene chloride).
Workup
- temperatureis heated
- temperatureheated
- waitto boiling for another 30 hours
- concentrationThen the reaction mixture is concentrated
- custompurified by flash chromatography (silica gel; methylene chloride)
Sources & evidence
- ORD record
- ord-6650bc2d3dba4efe8a9d1de39de56cee
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06479524B1
Reaction notes
Loading…