HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604638Generated: November 2, 2026
Sodium Chloride → 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid
https://huagongshe.com/reaction/1604638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Sodium Phosphate, Dibasic | HCID 24203 | — |
| Reactant | 4-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole | HCID 19603806 | — |
| Reactant | Sodium hydrogen sulphide | HCID 86586439 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid | HCID 19603694 | 87.8% |
Reaction Steps
Sodium chloride (0.47 g) was added to a mixture of 4-tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole (0.41 g), sodium hydrogenphosphate 12 water (0.23 g) and 2-methyl-2-butane (0.69 ml) in a mixed solvent of water (3 ml), tetrahydrofuran (7.5 ml) and tert-butanol (12.6 ml). After 4 hours, aqueous sodium hydrogensulfide solution was added to the mixture. The resulting mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue was dissolved in 1N-sodium hydroxide and the solution was treated with carbon powder and acidified with diluted hydrochloric acid. The resulting precipitates were collected and washed with water to give 2-(4-tert-butylthiazol-2-yl)benzofuran-5-carboxylic acid (0.38 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05994378 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-aaac001678ab4cbca26d8747b33292d8 |
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| Source note | uspto-grants-1999_11 |
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