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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487692Generated: October 29, 2026

Hydrochloric Acid → 4-Tert-butyl-2-[5-(2-hydroxymethylphenylthiomethyl)benzofuran-2-yl]thiazole

https://huagongshe.com/reaction/487692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-Tert-butyl-2-[5-(2-carboxyphenylthiomethyl)benzofuran-2-yl]thiazoleHCID 19092732—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-Tert-butyl-2-[5-(2-hydroxymethylphenylthiomethyl)benzofuran-2-yl]thiazoleHCID 1909273571.6%

Reaction Steps

To a mixture of 4-tert-butyl-2-[5-(2-carboxyphenylthiomethyl)benzofuran-2-yl]thiazole (0.65 g) in tetrahydrofuran (10 ml), lithium aluminum hydride (0.12 g) was added under cooling with ice bath. After being stirred at ambient temperature for 5 hours, the resulting mixture was poured into a mixture of ice and diluted aqueous hydrochloric acid and extracted with toluene. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to column chromatography on silica gel and eluted with a mixture of ethyl acetate and toluene (1:9). The fractions containing object compound were combined and concentrated under reduced pressure to give 4-tert-butyl-2-[5-(2-hydroxymethylphenylthiomethyl)benzofuran-2-yl]thiazole (0.45 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296495
Source datasetuspto-grants-1994_03
ORD IDord-d6f3728273274dafbda171ab659c5b30
Source noteuspto-grants-1994_03