HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxybenzaldehyde → 3-(4-Ethoxybenzyloxy)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxybenzaldehyde | HCID 101 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 4-Ethoxybenzyl alcohol | HCID 80345 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(4-Ethoxybenzyloxy)benzaldehyde | HCID 19388223 | — |
Reaction Steps
Mix 4-ethoxybenzyl alcohol (3.35 g. 22 mmol), 3-hydroxybenzaldehyde (2.69 g, 22 mmol), triphenylphosphine (5.8 g, 22 mmol) and diethylazadicarboxylate (3.83 g, 22 mmol) in tetrahydrofuran (25 mL). Stir at room temperature under anhydrous atmosphere until the reaction is done. Concentrate the solution in vacuo and dilute with a small quantity of ethyl ether. Filter any precipitate and concentrate the filtrate in vacuo. Purify by silica gel chromatography to give 3-(4-ethoxybenzyloxy)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05248825 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-43a0aaa7336a47c9a189d7a4c5585e94 |
| Source note | uspto-grants-1993_09 |