HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → Dibenzyloxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dihydroxybenzaldehyde | HCID 90579 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Dibenzyloxybenzaldehyde | HCID 10870855 | — |
Reaction Steps
13.8 g of 2,3-dihydroxybenzaldehyde, 30.4 g of benzyl chloride and 17.3 g of powdered anhydrous potassium carbonate in 160 ml of anhydrous ethanol are boiled under reflux with exclusion of moisture for 6 hours. The reaction solution is filtered, washing with ethanol, and the filtrate is evaporated in vacuo. On digestion of the residue with diisopropyl ether the known desired compound crystallizes and as white needles (M.p. 89°-91° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04797471 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-551534122ec6446d96eac137c4d0f25c |
| Source note | uspto-grants-1989_01 |