HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801689Generated: October 31, 2026
Acetone → 3,4-Bis(2-methoxyethoxy)benzaldehyde
https://huagongshe.com/reaction/1801689
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Iodo-2-methoxyethane | HCID 79136 | — |
| Product | 3,4-Bis(2-methoxyethoxy)benzaldehyde | HCID 16063391 | 47% |
Reaction Steps
80.0 g (0.57 mol) of 3,4-dihydroxy benzaldehyde and 800.0 ml of acetone were charged into 2.0 L4 necked round bottom flask, connect to a mechanical stirrer, thermo meter socket and condenser at 25-30° C. Reaction mass was stirred for 20 min. 324.0 g (1.74 mol) of 1-iodo-2-methoxy-ethane and 240.0 g (1.70 mol) of potassium carbonate were charged. Reaction mass was heated to reflux. Reaction mass temperature was maintained at reflux for 6 hours. Reaction mass temperature was cooled to 25-30° C. and inorganic solid was filtered. Acetone was completely distilled under vacuum at below 60° C. Remaining mass was diluted with 400.0 ml of DM water. Compound was extracted with 400.0 ml of ethyl acetate and organic layer was dried with sodiumsulphate. Ethyl acetate was completely distilled under vacuum and finally applied high vacuum at below 60° C. 69.20 g of crude product (Oil) was obtained (yield: 47.0% by theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08349847B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-334c7801aba444abb202fde45e495260 |
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| Source note | uspto-grants-2013_01 |
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