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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261429Generated: November 3, 2026

Acetic Acid → 3-Ethyl-4-hydroxy-5-methylbenzaldehyde

https://huagongshe.com/reaction/2261429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHexamethylenetetramineHCID 4101—
Reactant2-Ethyl-6-methylphenolHCID 519333—
SolventWaterHCID 962—
Product3-Ethyl-4-hydroxy-5-methylbenzaldehydeHCID 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 organic 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): δ 9.83 (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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07846964B2
Source datasetuspto-grants-2010_12
ORD IDord-4eff365c023c4be5bf3b3a854032b01b
Source noteuspto-grants-2010_12