HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Diethoxymethyl)benzaldehyde → Benzenemethanol, 4-(diethoxymethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Diethoxymethyl)benzaldehyde | HCID 595993 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Benzenemethanol, 4-(diethoxymethyl)- | HCID 11063705 | 90% |
Reaction Steps
To a solution of terephthalaldehyde mono(diethyl acetal) (1.9 ml, 9.6 mmol) in methanol (35 ml) was added sodium borohydride (1.1 g, 28.8 mmol) while cooling. After 5 minutes at room temperature the reaction was quenched with water (50 ml) and the mixture was extracted with ethyl acetate (2×50 ml). The combined extracts were washed with water and brine, dried over sodium sulfate and concentrated in vacuo, leaving title product as a colorless oil (1.81 g, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05061717 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-88817188c4c4442fb5c8c86cb7c37656 |
| Source note | uspto-grants-1991_10 |