HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 2-(2-Cyano-4-nitrobenzylidene)-3-ethylbenzothiazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Methyl-5-nitrobenzonitrile | HCID 350143 | — |
| Reactant | 2-(Phenylthio)benzothiazole | HCID 4346438 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(2-Cyano-4-nitrobenzylidene)-3-ethylbenzothiazoline | HCID 54451057 | — |
Reaction Steps
2-Phenylthiobenzothiazole ethiodide (3.99 g., 0.01 mole) and 2.00 g. (0.012 mole) of 2-cyano-4-nitrotoluene were dissolved in 25 ml. of acetonitrile and then 2.58 g. (0.02 mole) of diisopropyl ethylamine was added. The reaction mixture was refluxed two hours and then cooled for several hours. The green iridescent crystalline product was collected and washed with a small amount of acetonitrile. After drying 1.13 g. of product, m.p. 237°-9° (dec.) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04088497 |
| Source dataset | uspto-grants-1978_05 |
| ORD ID | ord-80aa2033a3f64d36ad92edc52cabcb0b |
| Source note | uspto-grants-1978_05 |