Hydrochloric Acid → HCID 57244169, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12](=[N:13][CH:14](Cl)[CH:15]([Cl:20])[C:16]([Cl:19])([Cl:18])[Cl:17])[C:11](=[O:22])[N:10]([CH3:23])[C:9]1=[O:24].[F:25][C:26]1[CH:32]=[CH:31][CH:30]=[CH:29][C:27]=1[NH2:28].C(N(CC)CC)C.Cl>C(#N)C.C(OCC)C>[F:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[N:8]1[C:12](=[N:13][CH:14]([NH:28][C:27]2[CH:29]=[CH:30][CH:31]=[CH:32][C:26]=2[F:25])[CH:15]([Cl:20])[C:16]([Cl:19])([Cl:18])[Cl:17])[C:11](=[O:22])[N:10]([CH3:23])[C:9]1=[O:24]Participants
7
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
In this example 0.02 mol of 1-(2-fluorophenyl)-3-methyl-5-(1,2,3,3,3-pentachloropropyl)imino-1,3-diazolidine-2,4-dione is dissolved in 20 ml of acetonitrile and then 0.02 of mol of 2-fluoroaniline is added. After about 10 minutes, triethylamine is added to neutralize the byproduct HCl produced by the reaction. The mixture is stirred for five hours and 20 ml of ethyl ether is then added. The mixture is filtered and the filtrate evaporated under high vacuum affording 1-(2-fluorophenyl)-3-methyl-5-(1-2'-fluorophenylamino-2,3,3,3-tetrachloropropyl)imino-1,3-diazolidine-2,4-dione.
Workup
- customproduced by the reaction
- filtrationThe mixture is filtered
- customthe filtrate evaporated under high vacuum
Sources & evidence
- ORD record
- ord-db75ff93ad034b18bb515748aba4d08b
- Source dataset
- uspto-grants-1981_02
- Patent number
- US04248620
Reaction notes
Loading…