HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370116Generated: October 30, 2026
3-Bromo-4-methoxybenzaldehyde → (3-Bromo-4-methoxyphenyl)methanol
https://huagongshe.com/reaction/1370116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromo-4-methoxybenzaldehyde | HCID 98662 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (3-Bromo-4-methoxyphenyl)methanol | HCID 13551346 | 99.1% |
Reaction Steps
To a solution of 3-bromo-4-methoxybenzaldehyde (4.98 g) in ethanol (50 mL) and tetrahydrofuran (10 mL) was added sodium borohydride (1.31 g) under ice-water cooling. The mixture was stirred at 0° C. for 2 hours. After evaporation of the solvent, the residue was partitioned between ethyl acetate and water. The separated organic layer was washed successively with water and brine, and dried over magnesium sulfate. The organic layer was evaporated in vacuo to give 3-bromo-4-methoxybenzyl alcohol as a colorless oil (4.98 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06582351B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-7f78ab457c67489ab445aa5a1d7bd82d |
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| Source note | uspto-grants-2003_06 |
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