HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → Benzyl 3-allyloxy-4-nitro-benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Hydroxy-4-nitrobenzoic acid benzyl ester | HCID 14986435 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Benzyl 3-allyloxy-4-nitro-benzoate | HCID 68107115 | 94.2% |
Reaction Steps
Benzyl 3-hydroxy-4-nitro-benzoate 29a (4.50 g, 16.47 mmol) was dissolved in 75 mL of anhydrous acetonitrile. The resulting solution was added with potassium carbonate (6.83 g, 49.41 mmol) and 3-bromopropene (2.9 mL, 32.94 mmol) successively, heated to reflux for 3 hours, then filtered. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound benzyl 3-allyloxy-4-nitro-benzoate 29b (4.86 g, yield: 94.2%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691822B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-53317d265ba04b569e60309df7e53e78 |
| Source note | uspto-grants-2014_04 |