HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364719Generated: November 1, 2026
Water → 7-Amino-2,3-dihydrobenzofuran-4-carboxylic acid
https://huagongshe.com/reaction/2364719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | Methyl 7-amino-2,3-dihydrobenzofuran-4-carboxylate | HCID 68107686 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-Amino-2,3-dihydrobenzofuran-4-carboxylic acid | HCID 24968336 | 80% |
Reaction Steps
Methyl 7-amino-2,3-dihydrobenzofuran-4-carboxylate 1g (2.30 g, 11.90 mmol) was dissolved in 80 mL of the mixture solvent of methanol and tetrahydrofuran (V/V=1:1) followed by the addition of a 1 M solution of lithium hydroxide solution (47.6 mL, 47.60 mmol) in tetrahydrofuran. The reaction solution was heated to reflux for 5 hours, then cooled down to room temperature, stirred for 12 hours. The reaction solution was added with 20 mL of water and concentrated under reduced pressure. The resulting residue was added with 100 mL of water, extracted with ethyl acetate (50 mL×2), the combined aqueous phase was added dropwise with 1 M hydrochloric acid to adjust pH to 3 resulting in the formation of precipitate. The precipitate was filtered to obtain the title compound 7-amino-2,3-dihydrobenzofuran-4-carboxylic acid 22e (1.70 g, yield: 80.0%) as a gary solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691822B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-3e646b25477c4414b2b8dccbf0b0d132 |
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| Source note | uspto-grants-2014_04 |
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