HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982472Generated: November 1, 2026
2-Hydroxy-5-methoxybenzaldehyde → 2-(hydroxymethyl)-4-methoxyphenol
https://huagongshe.com/reaction/1982472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Hydroxy-5-methoxybenzaldehyde | HCID 95695 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Diethylether hexane | HCID 21584099 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(hydroxymethyl)-4-methoxyphenol | HCID 480253 | 70% |
Reaction Steps
To a suspension of sodium borohydride (2.50 g, 65.8 mmol) in ethanol (100 mL) at 5° C. was added a solution of 2-hydroxy-5-methoxybenzaldehyde (10.00 g, 65.8 mmol) in ethanol (35 mL) dropwise. Upon completion of the addition the reaction mixture was allowed to stir for ten minutes then quenched by the dropwise addition of 10% aqueous acetic acid (75 mL). The ethanol was removed by concentration in vacuo and the resulting mixture poured into water (250 mL) and extracted with ethylacetate (3×100 mL). The combined extracts were washed sequentially with saturated sodium bicarbonate (50 mL), and brine (3×100 mL). The organic extract was dried (Na2SO4) and concentrated to afford a crude product (8.75 g). Trituration with hexane:ether (3:2, 25 mL) afforded 2-hydroxy-5-methoxybenzyl alcohol (7.00 g, 70%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04596828 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-ac36c031a5964613aba1d74687b7b2f4 |
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| Source note | uspto-grants-1986_06 |
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