HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethylammonium chloride → 2-(4-Nitrophenylimino)-1,3-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethylammonium chloride | HCID 13368 | — |
| Reactant | Benzene, 1-isothiocyanato-4-nitro- | HCID 75044 | — |
| Product | 2-(4-Nitrophenylimino)-1,3-thiazolidine | HCID 178526683 | — |
Reaction Steps
2-Chloroethylammonium chloride (Entry 1) was reacted with 4-nitrophenyl isothiocyanate according to Method C1a to give 2-(4-nitrophenylimino) -1,3-thiazolidine, which was reacted with isobutyl bromide according to Method D2a to give 2-(4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-9c2c3adbfc094af49dee06f5e44b302e |
| Source note | uspto-grants-2002_03 |