HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 851851Generated: October 26, 2026
Hydrochloric Acid → 3-Hydroxy-2-methoxy-1,2-diphenylpropan-1-one
https://huagongshe.com/reaction/851851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Methyl Benzoin | HCID 98097 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Hydroxy-2-methoxy-1,2-diphenylpropan-1-one | HCID 21909513 | — |
Reaction Steps
Potassium hydroxide 0.4 g was dissolved in ethanol 5 mL and dimethyl sulfoxide 200 mL was further added to obtain a solution. Benzoin methyl ether 30 g (0.13 mol) was dissolved in the solution and paraformaldehyde 5 g (0.16 mol) was added and reacted at 40° C. for 3 hours under nitrogen current. After that, the reaction product was cooled to a room temperature and neutralized with a dilute hydrochloric acid and then saturated salt water 120 mL was added. The solution was extracted by ethyl acetate and the extracted liquid was washed with saturated salt water three times. The washed product was dried and concentrated by anhydrous magnesium sulfate and recrystallized by diethyl ether. α-methylol benzoin methyl ether (MBME) was obtained in such a manner.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07253131B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-7a309612a73f478487bc80aaed6533eb |
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| Source note | uspto-grants-2007_08 |
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