HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460926Generated: November 2, 2026
4-Hydroxybenzoic Acid → 4-[(10-Hydroxydecyl)oxy]benzoic acid
https://huagongshe.com/reaction/1460926
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1-Decanol, 10-chloro- | HCID 123526 | — |
| Catalyst | Potassium Iodide | HCID 4875 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-[(10-Hydroxydecyl)oxy]benzoic acid | HCID 19768954 | 58% |
Reaction Steps
A mixture of 4-hydroxybenzoic acid (69.0 g, 0.5 mol), 10-chloro-1-decanol (106 g, 0.55 mol), potassium hydroxide (75 g, 1.15 mol), potassium iodide (0.1 g), and absolute ethanol (300 mL) was heated to reflux with mechanical stirring for 18 h. The mixture was diluted with water (800 mL) and stirred 0.5 h at room temperature. The mixture was acidified with 12N hydrochloric acid (125 mL) and the mixture stirred for 5 h. The material was allowed to sit overnight and filtered. The solid was washed with water and air dried 4 days. The solid was recrystallized from tetrahydrofuran (300 mL) to give 4-(10-hydroxydecyloxy)benzoic acid (85.2 g, 58%): mp 115°-117° C.; NMR (CDCl3 +d6DMSO) 7.93(d, 2H), 6.85(d, 2H), 4.0(t, 2H), 3.52(t, 2H), 3.48(bs, 1H), 1.9-1.2(m, 16H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05073294 |
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| Source dataset | uspto-grants-1991_12 |
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| ORD ID | ord-b92e0395dd9344a1b3fcbfa11ed4fcf1 |
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| Source note | uspto-grants-1991_12 |
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