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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629166Generated: October 29, 2026

Isopropanol → 2-[(Propan-2-yl)oxy]thiophene

https://huagongshe.com/reaction/629166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantPotassium CyanideHCID 9032—
Reactant2-IodothiopheneHCID 18921—
ReactantSodiumHCID 5360545—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product2-[(Propan-2-yl)oxy]thiopheneHCID 2305805716%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a mixture of 10 mL anhydrous isopropanol and 5 mL anhydrous tetrahydrofuran under argon at room temperature was added sodium metal (350 mg, 15.22 mmol). The resulting mixture was stirred vigorously at 35° C. until all the sodium metal was consumed (ca. 20 minutes). Copper(I) iodide (386 mg, 2.03 mmol) and 2-iodothiophene (2.13 g, 10.14 mmol) were added and the resulting suspension heated to 90° C. and stirred vigorously for 16 h. After cooling to room temperature, 20 mL of 0.5 M potassium cyanide aqueous solution was added and the resulting mixture stirred for 30 minutes. Organics were extracted with hexanes (2×75 mL), washed with water (3×50 mL) and brine (50 mL), dried over magnesium sulfate, filtered and concentrated. The residue was subjected to chromatography on silica gel (100% hexanes) to give 2-isopropoxythiophene (250 mg, 16%). Used without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315495B2
Source datasetuspto-grants-2016_04
ORD IDord-0b15eb8bc77b498188514a7e0b5c4649
Source noteuspto-grants-2016_04