HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857899Generated: November 1, 2026
Hydrochloric Acid → HCID 178455777, compound
https://huagongshe.com/reaction/1857899
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methylparaben | HCID 7456 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178455729 | HCID 178455729 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178455777 | HCID 178455777 | 57.5% |
Reaction Steps
A solution of potassium hydroxide (56.1 g) dissolved in 30 ml of water, and methyl 4-hydroxybenzoate (152 g) were suspended in 1500 ml of ethyleneglycolmonoethylether. To this mixture was dropped trans-4-ethylcyclohexylmethylbromide (200 g), and then the mixture formed was stirred under reflux for 4 hours. After cooling to room temperature, a solution of sodium hydroxide (80 g) dissolved in water (400 ml) was added with stirring and was refluxed for 2 hours. After the reaction was completed, the mixture was cooled, added with diluted hydrochloric acid (1 liter), and extracted with toluene (5 liters). The organic layer separated was washed with water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to obtain 4-(trans-4-ethylcyclohexylmethoxy)benzoic acid (147 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06149990 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-067b0ae94b564ff0bf98ec824aa11276 |
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| Source note | uspto-grants-2000_11 |
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