HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178433102, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 58453093 | HCID 58453093 | — |
| Product | HCID 178433102 | HCID 178433102 | 93% |
Reaction Steps
To acetonitrile (5 ml) solution of 1-methyl-1H-pyrazole-5-yl 2-methyl-6-(1H-1,2,4-triazol-1-yl)nicotinate (0.19 g, 0.65 mmol) and triethylamine (0.13 g, 1.29 mmol) , a catalytic amount of acetone cyanohydrin was added. The obtained solution was stirred at room temperature around the clock. Volatile materials were evaporated under reduced pressure from the obtained reaction solution, and the obtained residue was made acidic with citric acid aqueous solution, and was extracted with ethyl acetate. After washing the obtained organic layer with water, the organic layer was dried with magnesium sulfate and concentrated to obtain the desired product (0.18 g, yield 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08658798B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-cf6f2f04372548878a0f820d5df82279 |
| Source note | uspto-grants-2014_02 |