HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964875Generated: October 30, 2026
Potassium Carbonate → 4-(3-Formylphenoxy)butanoic acid
https://huagongshe.com/reaction/964875
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 4-(3-formylphenoxy)butanoate | HCID 10466631 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 4-(3-Formylphenoxy)butanoic acid | HCID 16495682 | 92.8% |
Reaction Steps
A solution of 385 mg (1.63 mmol) of 4-(3-formylphenoxy)butanoic acid, ethyl ester and 850 mg (6.15 mmol) of potassium carbonate is stirred in 6 mL of methanol/water (3:2) at room temperature for 8 hours. The solution is then concentrated in vacuo. The residue is dissolved in 10 mL of 0.1N sodium hydroxide solution and washed with 20 mL of ether. The aqueous layer is separated and acidified with sodium bisulfate and extracted with ethyl acetate. The organic layer is washed with saturated sodium chloride solution, then dried over magnesium sulfate. The mixture is then filtered and concentrated in vacuo to give 315 mg of 4-(3-formylphenoxy)butanoic acid as a white solid. The product is utilized in the next reaction without further purification. m.p. 62°-63°; the 1H NMR (300 MHz, CDCl3) is consistent with the desired product; IR (KBr) 3400, 3000, 1700, 1690, 1590 cm-1 ; MS (CI low res) m/e 209 (M+H), 191, 123.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773001 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-401399a1e96e44888487b2114fed6821 |
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| Source note | uspto-grants-1998_06 |
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