HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603750Generated: October 31, 2026
4-Hydroxybenzaldehyde → HCID 86754837, compound
https://huagongshe.com/reaction/1603750
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 3840273 | HCID 3840273 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86754837 | HCID 86754837 | 82.2% |
Reaction Steps
Then, 3.20 g of {1-(4-methoxyphenyl)-2-pyrrolidon-4-yl}methyl methanesulfonate and 1.4 g of 4-hydroxybenzaldehyde were dissolved in 32 ml of anhydrous N,N-dimethylformamide, to which 1.92 g of anhydrous potassium carbonate were added. The resultant mixture was stirred at 70° C. for 15 hours. The reaction mixture was filtered and the filtrate was concentrated. The thus-obtained residue was extracted with ethyl acetate. The extract was washed with water, dried over magnesium sulfate and then filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to chromatography on a silica gel column and then purified using gradient elution with hexane-ethyl acetate, whereby 2.86 g of the title compound were obtained (yield: 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05990139 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-ccfc9cb407734f219b3e8fd948de2b50 |
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| Source note | uspto-grants-1999_11 |
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