HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Benzyl tetrahydro-2H-pyran-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxane-4-carboxylic acid | HCID 219302 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzyl tetrahydro-2H-pyran-4-carboxylate | HCID 23131611 | 94% |
Reaction Steps
To a mixture of tetrahydro-2H-pyran-4-carboxylic acid (4.8 g) and potassium carbonate (7.6 g) and DMF (73 mL) was added dropwise benzyl bromide (4.6 mL) at 0° C. The reaction mixture was stirred at room temperature for one day, diluted with ice water, and extracted with ethyl acetate. The extract was washed with water, 0.5N hydrochloric acid, water and saturated brine, dried and concentrated under reduced pressure. The obtained residue was separated and purified by silica gel column chromatography (solvent gradient; 0→20% ethyl acetate/hexane) to give benzyl tetrahydro-2H-pyran-4-carboxylate (7.6 g, 94%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592454B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-b9e07990e8894571ab7ff17da0a066a5 |
| Source note | uspto-grants-2013_11 |