HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 647898Generated: October 30, 2026
Potassium Hydroxide → HCID 13092093, compound
https://huagongshe.com/reaction/647898
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 5-(2-formyl-3-benzyloxyphenoxy)pentanoate | HCID 20271552 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13092093 | HCID 13092093 | — |
Reaction Steps
A mixture of ethyl 5-(2-formyl-3-benzyloxyphenoxy)pentanoate (3.61 g, 0.01 M), potassium hydroxide (1.19 g, 0.021 M) and ethanol (40 ml) were stirred at 50°-60° C. for 5 hours. The ethanol was then removed in vacuo, the residue dissolved in water (50 ml) and the solution extracted with ether (2×80 ml). The aqueous layer was then acidified by the addition of 2 N aqueous hydrochloric acid and the product extracted with ether (3×50 ml), and the combined extracts washed with water to neutrality, dried, and concentrated in vacuo to give 5-(2-formyl-3-benzyloxyphenoxy) pentanoic acid, 3.0 g, 91% as a yellow oil which crystallised on standing. The crude solid was crystallised from benzene/petroleum spirit 30°-40° C. to give pale cream crystals m.p. 110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04410537 |
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| Source dataset | uspto-grants-1983_10 |
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| ORD ID | ord-843e341f804149c9942fa1ede9533c32 |
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| Source note | uspto-grants-1983_10 |
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