HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 13091191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 13091187 | HCID 13091187 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13091191 | HCID 13091191 | — |
Reaction Steps
A mixture of ethyl 5-(3,4-dihydroxyphenyl)-4-oxo-4H-pyran-2-carboxylate (3.0 g), anhydrous potassium carbonate (6.0 g) and benzyl bromide (3.0 ml) in dry DMF (30 ml) was stirred at room temperature for 2 hours and then filtered. The filtrate was cooled, acidified with 2 N hydrochloric acid (20 ml) and diluted with water (80 ml). The solid product was recrystallised from ethanol to give ethyl 5-(3,4-dibenzyloxyphenyl)-4-oxo-4H-pyran-2-carboxylate (mp 122°-125° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04364956 |
| Source dataset | uspto-grants-1982_12 |
| ORD ID | ord-456bf420db59460d96862d855b0a45ed |
| Source note | uspto-grants-1982_12 |