HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 9167Generated: October 23, 2026
Benzonitrile → (2-Amino-1,3-benzothiazol-6-yl)acetonitrile
https://huagongshe.com/en/reaction/9167
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzonitrile | HCID 7505 | — |
| Reactant | 4-Aminobenzonitrile | HCID 13396 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2-Amino-1,3-benzothiazol-6-yl)acetonitrile | HCID 21298164 | — |
Reaction Steps
2 grams of 4-aminobenzonitrile is dissolved in about 40 mL acetic acid and the solution is cooled to about 16° C. About 3.3 g of potassium thiocyanate is added and the flask is equipped with an addition funnel. The addition funnel is charged with about 2.7 g bromine and about 5 ml acetic acid. This dark solution is then added to the benzonitrile solution in a dropwise fashion under good agitation and allowed to stir for about 16 hours. The slurry is then drowned into water and filtered. The presscake is washed well with water, reslurried in dilute aqueous alkali and filtered. Again the presscake is washed well with water. After drying in vacuo, about 2 grams is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07091227B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-d0a3bdf85e9b4840981acc50d0208080 |
|---|
| Source note | uspto-grants-2006_08 |
|---|