HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569115Generated: October 30, 2026
Hydrochloric Acid → 5-(2,3-Dichloro-4-butyrylphenoxy)valeric acid
https://huagongshe.com/reaction/569115
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Ethyl 5-bromovalerate | HCID 84580 | — |
| Reactant | 1-(2,3-Dichloro-4-hydroxyphenyl)butan-1-one | HCID 14099856 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(2,3-Dichloro-4-butyrylphenoxy)valeric acid | HCID 13958737 | — |
Reaction Steps
A mixture of 2,3-dichloro-4-butyrylphenol (7 g, 0.03 mole), potassium carbonate (7.5 g, 0.054 mole) and ethyl 5-bromovalerate (9.5 g, 0.045 mole) in N,N-dimethylformamide (60 ml) were stirred and heated at 60° C. for 3 hours. The mixture was treated with 10 normal sodium hydroxide (12 ml) and water (50 ml), then stirred and heated on a steam bath for 2.5 hours. The solution was poured into ice water containing hydrochloric acid. The solid that separated was removed by filtration, washed with water and dried. The product (9.8 g) was recrystallized from butyl chloride to give 5-(2,3-dichloro-4-butyrylphenoxy)valeric acid, m.p. 102°-103° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731381 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-f3a482cf8cee4e90bed7cd50e28a4c7a |
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| Source note | uspto-grants-1988_03 |
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