HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196802Generated: October 25, 2026
Dimethylformamide → 5-Dodecylthiophene-2-carbaldehyde
https://huagongshe.com/reaction/1196802
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Dodecylthiophene | HCID 566347 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Dodecylthiophene-2-carbaldehyde | HCID 14985089 | 75.9% |
Reaction Steps
In a 1 liter-four-necked flask, 93.7 (1.28 mol) of N,N-dimethylformamide was placed and cooled to 5° C., followed by addition of 107.4 g (7.00×10-1 mol) of POCl3 in 15 min. below 10° C. under stirring. After stirring for 30 min. below 10° C., 160 g (6.35×10-1 mol) of 2-dodecylthiophene was added dropwise to the mixture in 10 min. at room temperature, followed by stirring for 1.5 hours and further stirring for 2.5 hours at 60° C. After the reaction, the reaction mixture was poured into 2 liters of iced water, subjected to 3 times of extraction with 500 ml of chloroform and washed 6 times with 500 ml of water. The organic layer was dried on CaCl2, followed by distilling-off of the solvent to obtain 237 g of a crude product. The crude product was subjected to reduced-pressure distillation in an atmosphere of nitrogen to obtain 135 g of a product (yield: 75.9%). b.p.: 160° C./0.6 mmHg
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05116530 |
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| Source dataset | uspto-grants-1992_05 |
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| ORD ID | ord-82136c440a0048babfec4f68af1cc474 |
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| Source note | uspto-grants-1992_05 |
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