Hydroxyamine hydrochloride → HCID 178518587, compound
Reaction equation
C([C:9]1[CH:14]=[C:13](Cl)[CH:12]=[CH:11][C:10]=1[NH:16][C:17]([NH:19][CH:20](C)C)=[O:18])(=O)C1C=CC=CC=1.Cl.N[OH:25]>C(O)C>[NH:16]1[C:10]2[C:9](=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:20]=[N+:19]([O-:25])[C:17]1=[O:18]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stirred mixture of 6.34 g (0.02 mole) of 1-(2-benzoyl-4-chlorophenyl)-3-isopropylurea and 4.17 g (0.06 mole) of hydroxylamine hydrochloride in 100 ml of ethanol was refluxed for 48 hr, and then cooled. The suspended crystals were collected on a filter, washed with alcohol, and then dried in air to give 4.60 g (84%) of 6-chloro-4-phenyl-(2(1H)-quinazolinone 3-oxide as yellow crystals, mp 267°-269° (dec.).
Workup
- temperaturewas refluxed for 48 hr
- temperaturecooled
- customThe suspended crystals were collected on a filter
- washwashed with alcohol
- customdried in air
Sources & evidence
- ORD record
- ord-12ec66151e09476ca7ce8e5d5b238fc4
- Source dataset
- uspto-grants-1981_03
- Patent number
- US04258187
Reaction notes
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