HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone Cyanohydrin → HCID 178463102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 8-bromoquinoline-5-carboxylic Acid | HCID 11021363 | — |
| Reactant | HCID 178418331 | HCID 178418331 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178463102 | HCID 178463102 | — |
Reaction Steps
1.00 g of 8-bromoquinoline-5-carboxylic acid, 0.44 g of 1-ethyl-5-hydroxypyrazole and 0.80 g of dicyclohexylcarbodiimide were stirred in 15 ml of acetonitrile at room temperature. After the addition of 0.2 ml of acetone cyanohydrin and 0.60 g of triethylamine, stirring was continued for 1.5 hours and the mixture was then poured into aqueous sodium carbonate solution. The alkaline phase was washed with ethyl acetate and diethyl ether and then acidified. The precipitate was filtered off under suction and the aqueous phase was extracted with ethyl acetate. This organic phase was dried and concentrated. The residue and the precipitate were combined.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262074B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-9fdd006d23c84e68816f4a08d800cf40 |
| Source note | uspto-grants-2001_07 |