HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341349Generated: October 29, 2026
2,3-Dimethylphenol → 4-(2,3-Dimethylphenoxy)butanoic acid
https://huagongshe.com/reaction/341349
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3-Dimethylphenol | HCID 10687 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 4-bromobutyrate | HCID 76300 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2,3-Dimethylphenoxy)butanoic acid | HCID 1622524 | — |
Reaction Steps
2,3-Dimethylphenol (24.5 g, 0.2 mol) was dissolved in 125 ml of anhydrous ethanol. Seventy five (75) ml of 21 wt % sodium ethoxide solution in ethanol (0.2 mol) was added to the solution. The mixture solution was stirred at room temperature for 10 min. Ethyl 4-bromobutyrate (40 g, 0.205 mol) was then added to the solution. The reaction mixture was refluxed at 80° C. for 24 h. The precipitate was filtered of. The filtrate was then mixed with a solution of sodium hydroxide (10 g, 0.25 mol) in 150 ml of water. The mixture was stirred at 70° C. for about 2 hours, and monitored with HPLC. The mixture was diluted with 150 ml of water and acidified to pH 1. Oily precipitate formed immediately. The precipitate was collected by decanting the supernatant and washed with water twice (100 ml×2). The oily precipitate solidified after being kept in water at room temperature overnight.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895777B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-02f2799bd0824bccadf0a76a277044e8 |
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| Source note | uspto-grants-2014_11 |
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