HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375924Generated: October 27, 2026
Triethylamine → 2-(1-Dodecynyl)-4-thiophenecarboxaldehyde
https://huagongshe.com/reaction/375924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Dodecyne | HCID 69821 | — |
| Reactant | 5-Bromothiophene-3-carbaldehyde | HCID 12284894 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(1-Dodecynyl)-4-thiophenecarboxaldehyde | HCID 18372976 | — |
Reaction Steps
A solution of 2-bromo-4-thiophenecarboxaldehyde (45.3 g), 1-dodecyne (43.4 g), and triethylamine (99 ml), in dry tetrahydrofuran (250 ml) was chilled to 5° C. and degassed under nitrogen. bis(Triphenylphosphine)palladium(II)chloride (1.66 g) and copper(I)iodide (0.23 g) were added to the reaction mixture. The mixture was degassed and stirred overnight, under nitrogen, as it was allowed to warm to room temperature. The precipitate was filtered off, washed with ethyl acetate, and the filtrate was evaporated. Ethyl acetate was added to the residue. The solution was washed with brine, dried over magnesium sulfate, filtered, and the filtrate was concentrated. The residue was chromatographed through a silica gel pad eluting with heptane/1% ethyl acetate. The appropriate fractions were collected and evaporated. The residue and that from a similar reaction on a 0.05 mole scale were combined and distilled to give 30.7 g (79.5%), bp 181°-185° C. @0.35 mm Hg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05488061 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-7f45390633e14f22bdec6ad69405b0cc |
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| Source note | uspto-grants-1996_01 |
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