p-Anisoyl chloride → HCID 86749787, compound
Reaction equation
C1(N[C:8]2[CH:13]=CC=CC=2N)C=CC=CC=1.[C:15]([Cl:25])(=[O:24])[C:16]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][CH:17]=1>C(OCC)C>[C:15]([Cl:25])(=[O:24])[C:16]1[CH:17]=[CH:18][C:19]([O:22][CH3:23])=[CH:20][CH:21]=1.[CH2:19]([O:22][CH2:13][CH3:8])[CH3:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of N-phenyl-o-phenylenediamine (10 mmol, 1.84 g) in 100 ml diethyl ether was stirred at room temperature as p-anisoyl chloride {1 mmol, 1.71 g) was added dropwise. The resulting mixture was stirred at room temperature for about 96 hours. A precipitate formed before half of the anisoyl chloride/diethyl ether was added.
Workup
- additionwas added dropwise
Sources & evidence
- ORD record
- ord-eaac4d8c75904c1eb6849e16764509be
- Source dataset
- uspto-grants-1996_09
- Patent number
- US05552426
Reaction notes
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