Aniline → AGN-PC-0NHP1N

HRID 1727241Notes

Reaction equation

HRID 1727241 reaction equation
[CH2:1]([C:3]1[O:4][C:5]2[C:11](=[O:12])[CH:10]=[CH:9][C:8](=[O:13])[C:6]=2[N:7]=1)[CH3:2].[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>C(O)C>[NH:14]([C:9]1[C:8](=[O:13])[C:6]2[N:7]=[C:3]([CH2:1][CH3:2])[O:4][C:5]=2[C:11](=[O:12])[CH:10]=1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1

Participants

4

Reactant 2

HCID 6115AnilineHCID 120715902-Ethyl-4,7-benzoxazoledione

Product 1

HCID 12071587AGN-PC-0NHP1N

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

A mixture of 2-ethyl-1,3-benzoxazole-4,7-dione (1 eq) and aniline (1.1 eq.) in ethanol is kept under string for 1 hour. The reaction medium turns to dark violet. After concentration, the residue is purified by medium pressure chromatography on silica in order to produce a violet-coloured powder. Melting point: 200° C.

Workup

  1. concentrationAfter concentration
  2. customthe residue is purified by medium pressure chromatography on silica in order
  3. customto produce a violet-coloured powder

Sources & evidence

ORD record
ord-7960ca578f5349db9ee05f85a9df403d
Source dataset
uspto-grants-2009_02
Patent number
US07495021B2

Reaction notes

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