HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19778Generated: October 26, 2026
Hydrochloric Acid → 4-Chloro-3-ethylbenzaldehyde
https://huagongshe.com/reaction/19778
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Bromo-1-chloro-2-ethylbenzene | HCID 44119401 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 4-Chloro-3-ethylbenzaldehyde | HCID 55265095 | 62.3% |
Reaction Steps
To a solution of 4.319 g of 4-bromo-1-chloro-2-ethyl-benzene (20 mmol) in 50 ml diethylether, cooled to 0° C., were added dropwise 12.3 ml of 1.6M n-BuLi in hexane. After 30 min. stirring at 0° C. and 2 h at RT, a solution of 2.43 ml DMF (31 mmol) in 10 ml diethylether was added dropwise (temperature raised from 20 to 28° C.). After 1 h additional stirring at RT, the reaction mixture was acidified with 2N HCl, diluted with 150 ml water and extracted with diethylether. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered off and concentrated in vacuo. The residue was purified by flash column chromatography (heptane/AcOEt: 95/5) to yield 2.1 g of a colorless oil. MS (ISP) 168.1 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07745477B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-71d96795f3b74acda950d9f94cb7eed1 |
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| Source note | uspto-grants-2010_06 |
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