HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739485Generated: October 26, 2026
Hydrochloric Acid → 2-Hydroxy-5-methylbenzyl alcohol
https://huagongshe.com/reaction/1739485
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-Methylsalicylic acid | HCID 6973 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Hydroxy-5-methylbenzyl alcohol | HCID 257452 | 68% |
Reaction Steps
To a suspension of LiAlH4 (2.5 g, 66 mmol) LiAlH4 in freshly distilled THF (8 ml) at 0° C. under argon, was added dropwise with stirring a solution of 5-methylsalicylic acid (5 g, 33 mmol) in freshly distilled THF (80 ml). Addition was complete in 0.75 hours and the reaction stirred at ambient temperature overnight. Careful addition of water (5 ml) was followed by the addition of ice (10 ml) and concentrated HCl (1 ml). The solvent was decanted and the residue treated with ethyl ether and ice water. The pH of the mixture was adjusted to pH 1 with concentrated HCl and the organic layer combined with the decanted solvent, washed with brine, dried (MgSO4) and evaporated. The residue was subjected to chromatography (eluant: ethyl ether/hexane) to give 2-hydroxymethyl-4-methylphenol as a white solid (3.1 g, 68%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05965741 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-3c128d959a9f45278fa6e5f06b5f80f1 |
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| Source note | uspto-grants-1999_10 |
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