HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 385238Generated: October 29, 2026
Water → 2,6-Diethyl-4-methylbenzyl alcohol
https://huagongshe.com/reaction/385238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 2,6-Diethyl-4-methylbenzaldehyde | HCID 22153798 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,6-Diethyl-4-methylbenzyl alcohol | HCID 66707540 | 92.2% |
Reaction Steps
A solution of 35.5 g (201.4 mmol) of 2,6-diethyl-4-methylbenzaldehyde, dissolved in 80 ml of diethyl ether is added dropwise to a suspension of 2.10 g (55.4 mmol) of lithium aluminium hydride in 200 ml of diethyl ether. The mixture is then heated at reflux for another 1 h. After cooling, the mixture is hydrolyzed with water and 10% strength sulphuric acid, the phases are separated and the aqueous phase is extracted two more times with diethyl ether. Drying (magnesium sulphate), distillative removal of the solvent and chromatography of the resulting crude product on silica gel (ethyl acetate/hexane=30:70) gives 33.10 g (92%) of 2,6-diethyl-4-methylbenzyl alcohol in the form of colourless crystals of m.p. 71-72° C. 1H-NMR (400 MHz, CDCl3): δ=1.22 (t, 6H), 2.30 (s, 3H), 2.74 (q, 4H), 4.71 (s, 2H), 6.90 (s, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367873B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-78777e775d634ce1bb2c4aa1c76e2e94 |
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| Source note | uspto-grants-2013_02 |
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