HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Isothiocyanato-2-(thiophen-2-yl)-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | 2-(Thiophen-2-yl)-1,3-benzothiazol-5-amine | HCID 21506699 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Isothiocyanato-2-(thiophen-2-yl)-1,3-benzothiazole | HCID 12781941 | — |
Reaction Steps
5-Amino-2-(2-thienyl)benzothiazole 7.0 g, 0.03 M is dissolved in 400 cc of tetrahydrofuran and 8.4 cc, 0.06 M, of triethylamine. Thiophosgene 2.3 cc, 0.03 M, is added, and the resulting mixture stirred at ambient temperature overnight. The solids which form are filtered, and washed with tetrahydrofuran. The filtrate is concentrated to dryness, and chromatographed on Alumina IV. The product is recrystallized from acetonitrile to yield 5.7 g of colorless needles, 70% of theory, m.p. 147°-149°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03985885 |
| Source dataset | uspto-grants-1976_10 |
| ORD ID | ord-67a8f48d06794da59e54157f6e05fde4 |
| Source note | uspto-grants-1976_10 |