HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichlorophenyl Isothiocyanate → 2-(2,3-Dichlorophenylimino)-3-cyclooctyl-1,3-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichlorophenyl Isothiocyanate | HCID 2796281 | — |
| Reactant | N-cyclooctyl-N-(2-chloroethyl)ammonium chloride | HCID 18316362 | — |
| Product | 2-(2,3-Dichlorophenylimino)-3-cyclooctyl-1,3-thiazolidine | HCID 18316171 | — |
Reaction Steps
2-Hydroxyethylamine was reacted with cyclooctyl bromide according to Method B2a to give N-cyclooctyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to give N-cyclooctyl-N-(2-chloroethyl)ammonium chloride. The chloroethylamine was reacted with 2,3-dichlorophenyl isothiocyanate to give 2-(2,3-dichlorophenylimino)-3-cyclooctyl-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-afe4030e78884949996ae2efa0f45ffc |
| Source note | uspto-grants-2002_03 |