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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 487703Generated: October 31, 2026

Acetic Anhydride → HCID 19092704, compound

https://huagongshe.com/reaction/487703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium AcetateHCID 517045—
Reactant4-Tert-butyl-2-(5-formylbenzofuran-2-yl)thiazoleHCID 19603806—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 19092704HCID 19092704100.6%

Reaction Steps

A mixture of 4-tert-butyl-2-(5-formylbenzofuran-2-yl)thiazole (4.46 g), hydroxylamine hydrochloride (3.96 g) and sodium acetate anhydrous (5.0 g) in acetic acid (40 ml) was stirred at ambient temperature for 3 hours. Subsequently, acetic anhydride (13 ml) was added to the mixture. After being stirred for 30 minutes at the same temperature, the reaction mixture was stirred at 120° C. for 2 hours. After being cooled, the mixture was poured into water, followed by collecting by filtration. The precipitates were washed with water and air-dried at ambient temperature. The crude products were washed with petroleum ether to give 4-tert-butyl-2-(5-cyanobenzofuran-2-yl)thiazole (4.44 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05296495
Source datasetuspto-grants-1994_03
ORD IDord-bbfe37a1501c4c938efb6808d2a2dc3a
Source noteuspto-grants-1994_03