Ethylene Glycol → HCID 178509023, compound
Reaction equation
[O:1]=[C:2]1[NH:6][C:5](=[NH:7])[CH2:4][S:3]1.[NH:8]=[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11](=N)[NH:10]1.C(O)CO>CO>[NH:8]=[C:9]1[C:17]2[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=2)[C:11](=[C:4]2[S:3][C:2](=[O:1])[NH:6][C:5]2=[NH:7])[NH:10]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
17.5 parts of 2-oxo-4-iminothiazolidine and 32 parts of the adduct of 1,3-diiminoisoindoline and ethylene glycol, in 400 parts of methanol, are refluxed for 5 hours. After the mixture has cooled, the product is filtered off, washed with methanol and dried. 33 parts of 1-imino-3-(2'-oxo-4'-iminothiazolidinylidene)-isoindoline (formula II, Z=°O) are obtained as a yellowish brown powder.
Workup
- temperatureAfter the mixture has cooled
- filtrationthe product is filtered off
- washwashed with methanol
- customdried
Sources & evidence
- ORD record
- ord-35ea67bd51284c1f9b36af32db24f4d1
- Source dataset
- uspto-grants-1982_03
- Patent number
- US04321390
Reaction notes
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