HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746424Generated: October 25, 2026
Hydrochloric Acid → 4-Cyclopentyloxy-3-hydroxybenzaldehyde
https://huagongshe.com/reaction/746424
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | 3,4-Dihydroxybenzaldehyde | HCID 8768 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Cyclopentyloxy-3-hydroxybenzaldehyde | HCID 16726149 | 67% |
Reaction Steps
A suspension of 3,4-dihydroxybenzaldehyde (5.0 gm, 0.0362 mol), anhydrous potassium carbonate (6.0 gm, 0.0434 mol) and cyclopentyl bromide (6.5 gm, 0.0434 mol) in dry DMF (50 ml) was heated and stirred at 80° C. for 24 hrs. Reaction mixture was then cooled and diluted with water (500 ml), acidified with 1N HCl and extracted with ethyl acetate (3×100 ml). The ethyl acetate extract was washed 5% sodium bicarbonate and brine and dried over anhydrous sodium sulfate. The dried extract on concentration afforded a residue which was purified by silica gel chromatography using 10% ethyl acetate in petroleum ether as the eluent to provide 5.0 gm of the title product as white solid. mp: 87-89° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393846B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-4371ba8580f9421dab962a92d0bbb1e4 |
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| Source note | uspto-grants-2008_07 |
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