HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629164Generated: November 1, 2026
Hydrochloric Acid → HCID 13025550, compound
https://huagongshe.com/reaction/629164
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (5-Bromothiophen-2-yl)methanol | HCID 11435467 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13025550 | HCID 13025550 | 89.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315495B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-841427134f52485d80a4cf104801996a |
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| Source note | uspto-grants-2016_04 |
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