HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloro-4-isothiocyanatobenzene → 2-(3,4-Dichlorophenylimino)-3-(cyclobutylmethyl)-1,3-thiazolidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloro-4-isothiocyanatobenzene | HCID 23065 | — |
| Reactant | N-cyclobutylmethyl-N-(2-chloroethyl)ammonium chloride | HCID 18316353 | — |
| Product | 2-(3,4-Dichlorophenylimino)-3-(cyclobutylmethyl)-1,3-thiazolidine | HCID 18316044 | — |
Reaction Steps
2-Hydroxyethylamine was reacted with cyclobutylmethyl bromide according to Method B2a to give N-cyclobutylmethyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to give N-cyclobutylmethyl-N-(2-chloroethyl)ammonium chloride. The chloroethylamine was reacted with 3,4-dichlorophenyl isothiocyanate to give 2-(3,4-dichlorophenylimino)-3-(cyclobutylmethyl)-1,3-thiazolidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353006B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-cfd7ff92352e4f07a34b7f9d8114bc0c |
| Source note | uspto-grants-2002_03 |