HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 86714061, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86714062 | HCID 86714062 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86714061 | HCID 86714061 | 77.7% |
Reaction Steps
In a mixture of crude 3-allyl-5-bromo-2-chloro-4-mercaptobenzonitrile and K2CO3 (1.79 g, 12.9 mmol) in CH3CN (80 mL), allylbromide (1.12 mL, 12.9 mmol) was added dropwise. The reaction mixture was stirred overnight at room temperature, and then filtered off. The resulting solution was evaporated and purified by silica gel chromatography to give the desired product 94 (1.1 g, 77.7% overall yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09034921B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-3f039f92f70b43839b8a46a05969e17c |
| Source note | uspto-grants-2015_05 |