HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070840Generated: October 25, 2026
Hydrochloric Acid → 3-Methoxythiophene-2-carboxylic acid
https://huagongshe.com/reaction/1070840
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Methyl 3-methoxythiophene-2-carboxylate | HCID 701637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methoxythiophene-2-carboxylic acid | HCID 1483475 | 100.3% |
Reaction Steps
To a solution of methyl 3-methoxythiophene carboxylate (2.0 g, 11.6 mmol) in 20 mL of THF at room temperature was added dropwise a 1.0 M sodium hydroxide aqueous solution (17.0 mL, 17.0 mmol). After addition, the mixture was heated to 75° C. (oil bath temperature) and continued for 18 h. The mixture was cooled to room temperature, treated with a 1.0 M hydrochloride aqueous solution until pH approximately being 2. The acidified mixture was extracted with 100 mL of CH2Cl2—CH3CN (1:1, v/v), 50 mL of CH2Cl2, and 50 mL of CH3CN. The combined organic extracts were washed with brine (30 mL), dried over Na2SO4, and concentrated under reduced pressure to a solid, which was further dried on high vacuum, yielding 1.84 g (100%) of 3-methoxythiophene carboxylic acid (MH+=159.0).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06903131B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-7d13398bb5a048d594b04e21531bd4b8 |
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| Source note | uspto-grants-2005_06 |
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