HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Bromoacetyl)benzonitrile → HCID 86618595, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Bromoacetyl)benzonitrile | HCID 98654 | — |
| Reactant | HCID 86618597 | HCID 86618597 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86618595 | HCID 86618595 | 81.2% |
Reaction Steps
A mixture of N-(2-hydroxy-1,1-dimethylpropyl)thiourea (720 mg, 4.4 mmol), prepared in the previous step, and 2-bromo-4′-cyano-acetophenone (980 mg, 4.4 mmol) in 20 mL of ethanol was heated under nitrogen to dissolve all of the solids. The reaction was allowed to come to room temperature and then stirred at room temperature overnight. The solid was collected by filtration and dried under reduced pressure to give 4-{2-[(2-hydroxy-1,1-dimethylpropyl)amino]-1,3-thiazol-4-yl}benzonitrile hydrobromide (1.3157 g, 81%) as a white solid, mp 208-210° C.; MS (ES) m/z 286.0 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618990B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-279b71fa289a456dbbbbadba29bd3d56 |
| Source note | uspto-grants-2009_11 |