HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-Acetamidosalicylic acid allyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-Acetamidosalicylic acid | HCID 65509 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Acetamidosalicylic acid allyl ester | HCID 53959255 | 62,745.5% |
Reaction Steps
To a stirred suspension of sodium hydride (4.0 g of 60%, 0.1 mmol) in 25 mL DMF was added dropwise a solution of 4-acetamidosalicylic acid (19.5 g, 0.1 mmol) in 50 mL DMF. After the evolution of hydrogen was over, allyl bromide (12.1 g, 0.1 mmol) was added and the mixture was stirred for 8.6 hours. DMF was removed in vacuo and the residue crystallized from methanol/water to give 14.76 g (62.76%) of the title compound as a white solid, mp 156-8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05173486 |
| Source dataset | uspto-grants-1992_12 |
| ORD ID | ord-4ba4528ef2f64ac7ac8a794d6d9a3d7f |
| Source note | uspto-grants-1992_12 |