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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium Phosphate, DibasicHCID 24203—
Reactant4-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazoleHCID 19603806—
ReactantSodium hydrogen sulphideHCID 86586439—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Tert-butylthiazol-2-yl)benzofuran-5-carboxylic acidHCID 1960369487.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994378
Source datasetuspto-grants-1999_11
ORD IDord-aaac001678ab4cbca26d8747b33292d8
Source noteuspto-grants-1999_11