HuagongsheHuagongshe Chemistry Print Report · For research reference only
Terephthalaldehyde → 4-(Hydroxymethyl)benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Terephthalaldehyde | HCID 12173 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Hydroxymethyl)benzaldehyde | HCID 556330 | 51% |
Reaction Steps
First, 2.06 g of terephthalaldehyde and 20 ml of ethanol were placed in a reaction vessel, to which 0.15 g of sodium borohydride was slowly added with stirring under ice cooling. After stirring at room temperature for 12 hours, the ethanol was evaporated. The residue was poured into diluted hydrochloric acid, and extracted with ethyl acetate. The ethyl acetate layer was washed twice with water, dried over anhydrous magnesium sulfate, and concentrated to give a crude product. This crude product was subjected to silica gel chromatography, which afforded 1.06 g (yield, 51%) of p-(hydroxymethyl)benzaldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06448444B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-3e312da4c4974e4884c6d02dce0b9a0d |
| Source note | uspto-grants-2002_09 |