HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016776Generated: October 30, 2026
Dimethylformamide → 3-Ethyl-4-methoxybenzaldehyde
https://huagongshe.com/reaction/1016776
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | 4-Bromo-2-ethyl-1-methoxybenzene | HCID 13301602 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Ethyl-4-methoxybenzaldehyde | HCID 22039772 | 42.4% |
Reaction Steps
A solution of 4-bromo-2-ethyl-1-methoxybenzene (J. Chem. Soc., Perkin Trans. 1, 1987, 1423; 2.13 g, 9.9 mmol) in THF (30 ml) was cooled to −78° C. A 1.6M solution of n-BuLi in hexane (7.42 ml, 11.9 mmol) was added slowly and the mixture was stirred for 1.5 h. at −78° C. The mixture was warmed slowly to −10° C. and subsequently again cooled to −78° C. DMF (2.29 ml, 29.7 mmol) was added slowly and the mixture was stirred for 1 h. at −78° C. and for 1 h. at 0° C. The reaction mixture was poured into ice-cold 3M HCl and extracted with diethyl ether. The organic phase was dried and filtered, and the filtrate was concentrated. The residue was purified by chromatography (SiO2, hexane/EtOAc 8:1=>2:1). There were obtained 690 mg (42%) of 3-ethyl-4-methoxy-benzaldehyde as a yellowish liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06476264B2 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-d35dbbf430d441478259eb0344af3100 |
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| Source note | uspto-grants-2002_11 |
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