Water → HCID 20434024, compound
Reaction equation
S(Cl)([Cl:4])(=O)=O.[Cl:6][C:7]1[CH:8]=[C:9]([CH:27]=[CH:28][C:29]=1[Cl:30])[CH2:10][N:11]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[C:13]2([C:23](=[O:24])[NH:22][C:21](=[O:25])[NH:20]2)[C:12]1=[O:26].O>C(O)(=O)C>[Cl:6][C:7]1[CH:8]=[C:9]([CH:27]=[CH:28][C:29]=1[Cl:30])[CH2:10][N:11]1[C:19]2[C:14](=[CH:15][C:16]([Cl:4])=[CH:17][CH:18]=2)[C:13]2([C:23](=[O:24])[NH:22][C:21](=[O:25])[NH:20]2)[C:12]1=[O:26]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Sulphuryl chloride (16.0 ml.) was added during 10 minutes to a stirred mixture of 1'-(3,4-dichlorobenzyl)spiro[imidazolidine-4,3'-indoline]-2,2',5-trione (28.2 g.) in acetic acid (400 ml.). The mixture obtained was then stirred at 60°-65° C. for 40 minutes. The clear solution which formed was poured into water (3 l.). The solid which was precipitated was collected by filtration, washed with water and air-dried. Recrystallisation of the crude solid thus obtained from aqueous propan-2-ol gave 1'-(3,4-dichlorobenzyl)-5'-chlorospiro[imidazolidine-4,3'-indoline]-2,2',5-trione (15.4 g.), m.p. 257°-259° C.
Workup
- customThe mixture obtained
- customThe clear solution which formed
- customThe solid which was precipitated
- filtrationwas collected by filtration
- washwashed with water
- customair-dried
- customRecrystallisation of the crude solid
- customthus obtained from aqueous propan-2-ol
Sources & evidence
- ORD record
- ord-85c9a0bfb7fa478282bfc317323a6250
- Source dataset
- uspto-grants-1984_12
- Patent number
- US04490381
Reaction notes
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