HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-Allyloxy-3-allylbenzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 3-allyl-4-hydroxybenzoate | HCID 939882 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4-Allyloxy-3-allylbenzoic acid methyl ester | HCID 11241748 | 87% |
Reaction Steps
A solution of 3.04 g (15.8 mmol) of methyl 4-hydroxy-3-propenylbenzoate (Example 42, Step B) was refluxed with anhydrous potassium carbonate (4.37 g, 2 equiv) and allyl bromide (3.5 mL, 2.5 equiv) in acetone overnight. The mixture was filtered through Celite and the filter cake was washed with more acetone and dichloromethane. After removing the solvents, the resulting oil was distilled under high vacuum to give 3.2 g (87%) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05449682 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-b22475391e1f49d4aac5b3d4c518fd03 |
| Source note | uspto-grants-1995_09 |