HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2037342Generated: October 30, 2026
Acetic Acid → 3-Ethyl-4-hydroxy-5-methylbenzaldehyde
https://huagongshe.com/reaction/2037342
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hexamethylenetetramine | HCID 4101 | — |
| Reactant | 2-Ethyl-6-methylphenol | HCID 519333 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Ethyl-4-hydroxy-5-methylbenzaldehyde | HCID 23159210 | — |
Reaction Steps
A solution of 2-ethyl-6-methyl-phenol (8.40 g, 61.7 mmol) and hexamethylene tetraamine (12.97 g, 92.5 mmol) in acetic acid (60 mL) and water (14 mL) is heated to 115° C. The water is distilled off at 117° C. and collected with a Dean-Stark apparatus. Then the water separator is replaced by a reflux condensor and the mixture is refluxed for 3 h. The mixture is cooled to rt, diluted with water (100 mL) and extracted with EA. The org. extract is washed with sat. aq. NaHCO3, dried over MgSO4 and evaporated. The remaining solid is dissolved in EA and treated with heptane to initialize crystallisation. The solid material is collected and dried to give 3-ethyl-4-hydroxy-5-methyl-benzaldehyde (3.13 g) as a colourless crystalline powder, 1H NMR (CDCl3): δ9.83 (s, 1H), 7.58-7.53 (m, 2H), 5.30 (s br, 1H), 2.69 (q, J=7.6 Hz, 2H), 2.32 (s, 3H), 1.28 (t, J=7.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08575200B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f29d1cf891954890a839b99edc370686 |
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| Source note | uspto-grants-2013_11 |
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