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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 13679816HCID 13679816—
ReactantSodium ChloriteHCID 23668197—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product5-Phenoxy-2-thiophenecarboxylic acidHCID 2235050655%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599916B2
Source datasetuspto-grants-2003_07
ORD IDord-07d87fb8d44d4e1c93b590bc059a4314
Source noteuspto-grants-2003_07