HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromo-2-methylpropane → 2-(2-Methyl-4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | 2-Chloroethylammonium chloride | HCID 13368 | — |
| Reactant | 2-Methyl-4-nitrophenyl isothiocyanate | HCID 145621 | — |
| Product | 2-(2-Methyl-4-nitrophenylimino)-3-isobutyl-1,3-thiazolidine | HCID 18316064 | — |
Reaction Steps
2-Chloroethylammonium chloride (Entry 1) was reacted with 2-methyl-4-nitrophenyl isothiocyanate, which was reacted with isobutyl bromide according to Method D2a to give 2-(2-methyl-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-7bd3e815d99c47a49645b66ede2713fd |
| Source note | uspto-grants-2002_03 |