HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542392Generated: October 31, 2026
Hydroquinone → Phenol, 2-ethoxy-4-(methoxymethyl)-
https://huagongshe.com/reaction/542392
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | HCID 3732967 | HCID 3732967 | — |
| Product | Phenol, 2-ethoxy-4-(methoxymethyl)- | HCID 6453284 | 56.3% |
Reaction Steps
100 g of ethylvanillyl alcohol (4-hydroxy-3-ethoxybenzyl alcohol) are dissolved in 200 ml of methanol. The solution is treated with 10 g of sodium hydrogen sulphate and a knife tip of hydroquinone. The mixture is firstly heated to 50° C. for 2 minutes and left to cool again to room temperature. The methanolic solution is now poured into 85 ml of a saturated sodium hydrogen carbonate solution. The methyl alcohol is distilled off in vacuo, the residue is taken up in toluene, the organic solution is washed neutral with water and evaporated. The residue (95.5 g) is fractionally distilled. There are obtained 61.1 g of chemically and olfactorily pure 4-hydroxy-3-ethoxybenzyl methyl ether; b.p.=77° C./0.03 mmHg; d420 =1.1084; nD20 =1.529.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04657700 |
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| Source dataset | uspto-grants-1987_04 |
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| ORD ID | ord-437c75b7674c40bbb271caf90f3d3e76 |
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| Source note | uspto-grants-1987_04 |
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