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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629164Generated: November 1, 2026

Hydrochloric Acid → HCID 13025550, compound

https://huagongshe.com/reaction/629164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant(5-Bromothiophen-2-yl)methanolHCID 11435467—
SolventTetrahydrofuranHCID 8028—
ProductHCID 13025550HCID 1302555089.1%

Reaction Steps

To a solution of (5-bromothiophen-2-yl)methanol (460 mg, 2.38 mmol) in 5 mL anhydrous tetrahydrofuran at room temperature was added carefully hexanes-washed sodium hydride (60% in oil, 143 mg, 3.57 mmol). After stirring at room temperature for 30 minutes, methyl iodide (0.3 mL, 4.76 mmol) was added in a single portion and the reaction mixture stirred for 16 h at room temperature. The reaction mixture was poured into 20 mL of 0.2 N hydrochloric acid. Organics were extracted with 1:1 ether/hexanes (3×25 mL), washed with 30 mL each of 5% aqueous sodium bisulfite solution and brine, dried over magnesium sulfate, filtered and concentrated. The crude residue was subjected to chromatography on silica gel with gradient elution (2-3% ethyl acetate in hexanes) to give 2-bromo-5-(methoxymethyl)thiophene (439 mg, 89%) as an oil. Used without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315495B2
Source datasetuspto-grants-2016_04
ORD IDord-841427134f52485d80a4cf104801996a
Source noteuspto-grants-2016_04