HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 403010Erstellt: 24. Oktober 2026
3,4-Bis(benzyloxy)benzaldehyde → 3,4-Bis(benzyloxy)benzyl alcohol
https://huagongshe.com/de/reaction/403010
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 3,4-Bis(benzyloxy)benzaldehyde | HCID 79526 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 3,4-Bis(benzyloxy)benzyl alcohol | HCID 74338 | 97,5% |
Reaktionsschritte
3,4-Dibenzyloxybenzaldehyde (27) (22.0 mmol) was suspended in 100 mL of anhydrous methanol and cooled to 0° C. under argon. Sodium borohydride (33.0 mmol) was added in portions to the suspension and stirred for 1 h at the same temperature. The resulting solution was then stirred at room temperature overnight. The reaction mixture was evaporated to dryness and the residue was dissolved in ice-water and neutralized with HCl. The solution was then extracted with chloroform and the organic layer was washed successively with water, 10% NaHCO3 solution in water and brine. The organic layer was dried over anhydrous Na2SO4, filtered and evaporated to dryness to provide pure 3,4-Dibenzyloxybenzyl alcohol (28) in 97.5% yield.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08742139B2 |
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| Quelldatensatz | uspto-grants-2014_06 |
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| ORD ID | ord-17c46815fde54f19a6db355bcab2ae54 |
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| Quellennotiz | uspto-grants-2014_06 |
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