HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 5-Benzyloxy-2-methoxybenzyl alcohol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(Benzyloxy)-2-methoxybenzaldehyde | HCID 10966694 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Benzyloxy-2-methoxybenzyl alcohol | HCID 14333132 | 95% |
Reaction Steps
5-Benzyloxy-2-methoxybenzaldehyde (150.4 g) was suspended in methanol (600 ml) and to the gently warmed stirred mixture was added, in portions, sodium borohydride (15.0 g). The methanol was evaporated and the residue partitioned between dichloromethane and water. The organic layer was washed with water, then saturated sodium chloride, dried with anhydrous magnesium sulphate and evaporated to dryness. The residue crystallised from dichloromethane/petroleum spirit (40°-60° ) to give 5-benzyloxy-2-methoxybenzyl alcohol (143.8 g, 95%), m.p. 50°-51°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04766121 |
| Source dataset | uspto-grants-1988_08 |
| ORD ID | ord-91b15ab66d5f401eb351dbea3663074b |
| Source note | uspto-grants-1988_08 |