HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359638Generated: October 28, 2026
Sodium Hydroxide → 5-Phenoxy-2-thiophenecarboxylic acid
https://huagongshe.com/reaction/1359638
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13679816 | HCID 13679816 | — |
| Reactant | Sodium Chlorite | HCID 23668197 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Phenoxy-2-thiophenecarboxylic acid | HCID 22350506 | 55% |
Reaction Steps
5-Phenoxy-thiophene-2-carboxaldehyde (325 mg, 1.6 mmol) is dissolved in a mixture of THF (10 mL), t-BuOH (5 mL) and water (5 mL). NaH2PO4 (650 mg, 4.8 mmol) is added followed by NaClO2 (432 mg, 4.8 mmol). The resulting mixture is stirred for 24 hours at room temperature. Aqueous NaOH (2M, 5 mL) is added, and the organic solvents are removed in vacuo. The resulting aqueous suspension is poured into water (10 mL) and washed with ether (3×50 mL). The aqueous layer is acidified to pH<2 with 25% H2SO4 then washed with CH2Cl2 (3×50 mL). The combined organic washes are dried over Na2SO4, filtered and concentrated in vacuo. The crude product is dissolved in hot aqueous acetone and filtered. The solvents are gradually removed until a precipitate forms. The solid is collected by filtration and dried in vacuo to yield the desired product (192 mg, 55%). MS for C11H7O3S (ESI) (M−H)+ m/z 219.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06599916B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-07d87fb8d44d4e1c93b590bc059a4314 |
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| Source note | uspto-grants-2003_07 |
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