HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Chloride → 3,5-Difluoro-2,4-dibenzyloxybenzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3,5-Difluoro-2,4-dihydroxybenzaldehyde | HCID 18942327 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,5-Difluoro-2,4-dibenzyloxybenzaldehyde | HCID 18942322 | — |
Reaction Steps
To a 0.1M solution of Compound 13 (1.0 eq) in acetone is added benzyl chloride (4.0 eq) and anhydrous K2CO3 (7.0 eq). The mixture is heated to reflux for 8 hours and filtered. The filtrate is concentrated in vacuo, and the residue is dissolved in EtOAc. The resulting solution is washed with 3% HCl, washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residue is recrystallized from MeOH to yield Compound 23.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05830912 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-859e2011bfca461496c39b018267b274 |
| Source note | uspto-grants-1998_11 |