HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloro-2-isothiocyanatobenzene → 1-((3-Chloro-5-(trifluoromethyl)pyridin-2-yl)methyl)-3-(2-chlorophenyl)thiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloro-2-isothiocyanatobenzene | HCID 123171 | — |
| Reactant | 1-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]methanamine hydrochloride | HCID 11499744 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-((3-Chloro-5-(trifluoromethyl)pyridin-2-yl)methyl)-3-(2-chlorophenyl)thiourea | HCID 22637219 | — |
Reaction Steps
To a suspension of (3-chloro-5-trifluoromethyl-2-pyridyl)methylamine hydrochloride (0.12 g) and 2-chlorophenylisothiocyanate (0.09 g) in dry tetrahydrofuran (10 ml) was added 10 drops of triethylamine. The mixture was stirred at room temperature overnight. The solvent was removed by evaporation in vacuo and the residue extracted with ethyl acetate and washed with 2M hydrochloric acid. The layers were separated and the organic phase was evaporated to dryness to give the title product, m.p. 126° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06821992B1 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-adcdd127e4904a5c8fbdc0437588f93d |
| Source note | uspto-grants-2004_11 |