HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602716Generated: October 25, 2026
Protocatechuic Acid → Benzyl 3,4-dihydroxybenzoate
https://huagongshe.com/reaction/1602716
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Protocatechuic Acid | HCID 72 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Water | HCID 962 | — |
| Product | Benzyl 3,4-dihydroxybenzoate | HCID 16656541 | — |
Reaction Steps
A solution of sodium hydroxide (6.4 g) in water (40 ml) was added to a mixture of 3,4-dihydroxybenzoic acid (24.8 g) and DMF (200 ml) which had been cooled in an ice-bath. The mixture was stirred for 20 minutes and then benzyl bromide (19.1 ml) was added dropwise. After the addition was complete, the mixture was allowed to reach ambient temperature and was stirred for 20 hours. The mixture was then warmed to 50° C. for 2 hours. The solvent was removed by evaporation and the residue was partitioned between water (300 ml) and ethyl acetate (100 ml). The ethyl acetate layer was separated and the aqueous layer extracted with ethyl acetate (100 ml). The combined ethyl acetate extracts were washed with water (100 ml), saturated sodium hydrogen carbonate solution (100 ml), water (100 ml) and with saturated sodium chloride solution (100 ml) and dried (MgSO4). The solvent was removed by evaporation to give a brown solid which was crystallised from toluene to give benzyl 3,4-dihydroxybenzoate (19 g) as a solid; m.p. 147-149° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05981531 |
|---|
| Source dataset | uspto-grants-1999_11 |
|---|
| ORD ID | ord-df1752dc7e1c4b669aeb8d1f254d3b36 |
|---|
| Source note | uspto-grants-1999_11 |
|---|