HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 67128148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 86646365 | HCID 86646365 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67128148 | HCID 67128148 | — |
Reaction Steps
A solution of 2.5g (10.49 mmol) 2-fluoro-5-(tetrahydropyrane-2-yloxymethyl)-benzaldehyde in anhydrous methanol is mixed in portions with 0.60 g (15.7 mmol) sodium borohydride while stirring and stirred for another hour at room temperature. After adding water, extraction is performed using diethyl ether, and the organic phase is dried over sodium sulfate. After removing the solvent under vacuum, the benzyl alcohol is obtained in pure form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08273793B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-15fb6455c09b4dc99b2d741003aacf09 |
| Source note | uspto-grants-2012_09 |