HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944648Generated: October 29, 2026
Water → 4-(2,3,4-Trimethoxyphenyl)butanoic acid
https://huagongshe.com/reaction/1944648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 6-(2,3,4-Trimethoxyphenyl)-6-oxohexanoic acid | HCID 24727163 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(2,3,4-Trimethoxyphenyl)butanoic acid | HCID 43589091 | 78% |
Reaction Steps
17 g of sodium hydroxide was dissolved in 200 mL of methanol in a 1000 mL round bottom flask. The reaction mixture was cooled to room temperature and 66 (6.78 g, 22.90 mmol) was added followed by 60 mL of water and 300 mL of anhydrous methanol, and the reaction mixture was refluxed for 30 min. The solvent was evaporated under reduced pressure and the reaction mixture was neutralized with dilute hydrochloric acid and the reaction mixture was extracted with ether (200×3) and the combined organic phases were washed with water and dried over sodium sulfate and solvent evaporated under reduced pressure. The crude product was purified by column chromatography (30:70 EA:Hex) to yield 12.86 g of 57 as pale yellow colored oil (78%). Rf: 0.15 (40:60 EtOAc:Hexanes).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394859B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-050754c30f3140ea930720775c67378f |
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| Source note | uspto-grants-2013_03 |
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