HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenyl Isothiocyanate → HCID 20313842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenyl Isothiocyanate | HCID 7673 | — |
| Reactant | 5-Methoxy-1,2,3-benzothiadiazole | HCID 12494997 | — |
| Product | HCID 20313842 | HCID 20313842 | — |
Reaction Steps
A solution of 5-methoxy-1,2,3-benzothiadiazole (5 g) in 50 ml of phenyl isothiocyanate is heated at 220° C under an inert atmosphere until the evolution of nitrogen ceases (about two hours). The excess phenyl isothiocyanate is removed in vacuo. The resultant residue is chromatographed on silica gel (500 ml) eluting with pentane/dichloromethane (4:1). Fractions containing the desired product (Rf =0.2, silica gel, benzene) are combined and concentrated in vacuo. The resultant solid is recrystallized from pentane to yield 2.8 g of the title compound, melting point 58°-60° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04104467 |
| Source dataset | uspto-grants-1978_08 |
| ORD ID | ord-ad62bddbb94e4999ad2b9ee154c5a48d |
| Source note | uspto-grants-1978_08 |