HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 10118Generated: October 26, 2026
4-Hydroxybenzoic Acid → 4-(6-Hydroxyhexyloxy)benzoic acid
https://huagongshe.com/reaction/10118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzoic Acid | HCID 135 | — |
| Reactant | 6-Chloro-1-hexanol | HCID 74828 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 4-(6-Hydroxyhexyloxy)benzoic acid | HCID 3628413 | 80% |
Reaction Steps
Monomers in which the bulky organic group was a t-butyl group and the alkyl groups were hexyl groups were made as follows. 4-hydroxybenzoic acid was dissolved in 30% ethanolic KOH. About 1% of KI was added as a catalyst. The mixture was heated to about 60° C. and a stoichiometric amount of 6-chloro-1-hexanol was slowly added over about ½ hour. After refluxing the reaction mixture for extended period of time (2-15 hrs) the contents was cooled, the reaction mixture was filtered off, and the filtrate solvent was evaporated under vacuum. Water was added into the residue and acidified with HCl and the precipitate was filtered and crystallized with ethanol, yielding approximately an 80% 4-(6-hydroxyhexyloxy)-benzoic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07094358B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-dfe4ced729254e01be55cc9bea0175d5 |
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| Source note | uspto-grants-2006_08 |
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