HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593915Generated: November 1, 2026
4-Hydroxybenzoic Acid → 4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acid
https://huagongshe.com/reaction/1593915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-{[(6-Bromohexyl)oxy]methyl}-3-ethyloxetane | HCID 59207310 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-({6-[(3-Ethyloxetan-3-YL)methoxy]hexyl}oxy)benzoic acid | HCID 59767596 | 66.4% |
Reaction Steps
First stage: A solution prepared by dissolving 500 g of 3-[(6-bromohexyloxy)methyl]-3-ethyloxetane, 297 g of 4-hydoxybenzoic acid and 490 g of potassium carbonate in 3 L of dimethylforamide was stirred at 90° C. for 8 hours. After adding 4 L of water to the reaction mixture, it was extracted with 4 L of toluene. The organic layer was washed with water, and then the solvent was distilled off. Added to the resulting residue were 200 g of sodium hydroxide, 1 L of water and 2.5 L of ethanol, and the mixture was refluxed for 4 hours. Ethanol 1 L was distilled off at an atmospheric pressure, and then the solution was acidified by hydrochloric acid to obtain a slurry. The slurry was filtered and dried to thereby obtain 400 g of 4-[6-(3-ethyloxetane-3-ylmethoxy) hexyloxy]benzoic acid (melting point: 58.5° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07300604B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-5958c7f071e84ed7af3ac059efc2ff9c |
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| Source note | uspto-grants-2007_11 |
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