Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-Benzylbenzaldehyde | HCID 13102743 | — |
| Reactant | Diethylether water | HCID 21584184 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Benzylbenzyl alcohol | HCID 597613 | 93.6% |
Reaction Steps
3-Benzylbenzaldehyde (5.5 g) was dissolved in methanol (75 cm3) and cooled to 0° C. Sodium borohydride (1.29 g) was added gradually in small portions, and stirring was continued for one hour. The reaction mixture was cautiously poured into a water/diethyl ether mixture, and the resulting ethereal solution was washed with water and brine, and dried over anhydrous magnesium sulphate. Evaporation of the solvents under reduced pressure gave 3-benzylbenzyl alcohol as a pale yellow oil (5.2 g). The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05196610 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-c1e47ff332e743689be6b776dd985ec0 |
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| Source note | uspto-grants-1993_03 |
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