Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 59515212 | HCID 59515212 | — |
| Product | HCID 68646365 | HCID 68646365 | — |
Reaction Steps
NaBH4 (0.38 g, 10 mmol) was added to a solution of 2-bromo-3-(4-methoxy-benzyloxy)-benzaldehyde (1.59 g, 4.95 mmol) in EtOH (15 mL) at 0° C. (bath temp). The mixture was stirred at 0° C. (bath temp) for 1.5 h and then concentrated in vacuo. H2O (10 mL) was added and the aqueous layer was extracted with EtOAc (2×50 mL). The organic fractions were washed with brine (20 mL), dried (Na2SO4), and concentrated in vacuo to give the title compound as white solid: yield 1.50 g (94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895534B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-47b5de9a5ee9449a8d3e23afd7c54fd1 |
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| Source note | uspto-grants-2014_11 |
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