HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904471Generated: October 29, 2026
Diethyl Ether → 2,4-Dimethylthiophene-3-carbaldehyde
https://huagongshe.com/reaction/904471
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Bromo-2,4-dimethylthiophene | HCID 10631774 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 2,4-Dimethylthiophene-3-carbaldehyde | HCID 11147770 | — |
Reaction Steps
A solution of 15 g. (79.0 mmol) of 2,4-dimethyl-3-bromothiophene in 120 ml. of dry ether was cooled to -70° C. and 36 ml. of a hexane solution of n-butyl lithium (2.4 molar, 86.4 mmol) were added dropwise. The reaction mixture was allowed to warm up to -20° C. for 10 min., cooled again to -70° C. and then quenched by adding dropwise 15 g. (0.205 mol) of dimethylformamide. The mixture was stirred at room temperature overnight, poured into ice water, stirred for 15 min. and extracted four times with ether. The ether phase was washed with saturated sodium chloride solution, dried and evaporated. The resulting oily residue was distilled to yield 2,4-dimethylthiophene-3-carboxaldehyde, b.p. 50°-55° C./0.1 mm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04230872 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-3ebb462a37434efc8c3903babe0579c1 |
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| Source note | uspto-grants-1980_10 |
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