HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 744182Generated: October 30, 2026
Methylparaben → Methyl 4-(allyloxy)benzoate
https://huagongshe.com/reaction/744182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-(allyloxy)benzoate | HCID 4645407 | — |
Reaction Steps
To a nitrogen flushed 5 L three neck round bottom flask fitted with a mechanical stirrer, condenser, and a nitrogen inlet was charged 608 g (4 mol) of methyl 4-hydoxybenzoate, 520 ml (727 g, 6.00 mol, 1.5 eq) of allyl bromide, 663 g (9.6 mol of anhydrous potassium carbonate, and 2.3 L of acetone. The mixture was refluxed with vigorous stirring for 90 min. Additional potassium carbonate, (50 g) was added, and 25 g added again after an additional 50 min. After 20 min (total reaction time of 160 min), the suspension was allowed to cool to ambient temperature and stirred overnight. The mixture was filtered and the cake washed with 3 L of acetone. The solution was concentrated to obtain 788.6 g (theoretical yield 768.9 g) of a pale yellow, almost colorless oil which was used without purification in the next step. The product was a single spot on TLC (silica-1:1 EtOAc/Hex) and the NMR was consistent with methyl 4-allyloxybenzoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05559135 |
|---|
| Source dataset | uspto-grants-1996_09 |
|---|
| ORD ID | ord-2d37acd6f4b24333869c622c103d9fb2 |
|---|
| Source note | uspto-grants-1996_09 |
|---|