HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629165Generated: October 31, 2026
Hydrochloric Acid → HCID 13888631, compound
https://huagongshe.com/reaction/629165
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | HCID 13025550 | HCID 13025550 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | tetrahydrofuran HMPA | HCID 86583969 | — |
| Product | HCID 13888631 | HCID 13888631 | 31.1% |
Reaction Steps
To a solution of 2-bromo-5-(methoxymethyl)thiophene (439 mg, 2.12 mmol) in 6 mL of 9:1 tetrahydrofuran/hexamethylphosphoramide under argon at −78° C. was added n-butyllithium (0.93 mL, 2.5 M in hexanes) dropwise. After stirring for 2 minutes at −78° C., dimethylformamide (0.82 mL, 10.6 mmol) was added in a single portion and the reaction mixture was allowed to warm to room temperature before being poured into 30 mL of 1 N hydrochloric acid. Organics were extracted with 1:1 ether/hexanes (3×30 mL), washed with water (2×30 mL, brine (30 mL), dried over magnesium sulfate, filtered and concentrated. The crude residue was subjected to chromatography on silica gel with gradient elution (5-20% ethyl acetate in hexanes) to give 5-(methoxymethyl)thiophene-2-carbaldehyde (103 mg, 31%) 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-c4f0385284df4279a0d4347739bb5c17 |
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| Source note | uspto-grants-2016_04 |
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