HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694805Generated: October 26, 2026
Sulfuric Acid → 2-Chloro-6-ethylbenzaldehyde
https://huagongshe.com/reaction/1694805
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 178448975 | HCID 178448975 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Chloro-6-ethylbenzaldehyde | HCID 22613746 | 77% |
Reaction Steps
To a solution of 19.7 g (88.1 mmol) butyl-[1-(2-chloro-6-ethyl-phenyl)-meth-(E)-ylidene]-amine in 70 ml water at 0° C. was added dropwise 18.9 ml concentrated sulphuric acid. The mixture was then heated at reflux for 90 min before being cooled to room temperature and diluted with ethyl acetate. The mixture was then washed sequentially with water, saturated aqueous sodium bicarbonate solution, and saturated brine. The organic phase was dried over Na2SO4, filtered and concentrated in vacuo. The residue was purified by flash chromatography (silica gel, ethyl acetate/heptane 1:30) to afford 11.4 g (77%) of the title compound as a yellow oil. 1H-NMR (CDCl3): 1.22 (3H, t, CH3), 2.97 (2H, q, CH2), 7.20 (1H, d, ArH), 7.30 (1H, d, ArH), 7.39 (1H, dd, ArH), 10.65 (1H, s, CHO).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158668B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-b41f0e2f446f4d4db6bd5afbcd86beb4 |
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| Source note | uspto-grants-2012_04 |
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