Anthranilamide → HCID 11345158, compound
Reaction equation
[NH2:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5].[CH2:11](Cl)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>O>[CH2:11]([NH:1][C:2]1[CH:10]=[CH:9][CH:8]=[CH:7][C:3]=1[C:4]([NH2:6])=[O:5])[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a hot solution of 20 g Na OHin 1250 ml water was added 68 g 2-aminobenzamide followed by 58 ml benzyl chloride. The mixture was refluxed 20 minutes, cooled and the solid filtered and washed with water. The product was recrystallized from 95% alcohol to give 62 g, m.169-73°.
Workup
- temperatureThe mixture was refluxed 20 minutes
- temperaturecooled
- filtrationthe solid filtered
- washwashed with water
- customThe product was recrystallized from 95% alcohol
- customto give 62 g, m
- custom169-73°
Sources & evidence
- ORD record
- ord-3939ffe401a54a14a08aa648fbedeb04
- Source dataset
- uspto-grants-1977_11
- Patent number
- US04060526
Reaction notes
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