HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 508580Generated: November 2, 2026
Hydrochloric Acid → HCID 71294558, compound
https://huagongshe.com/reaction/508580
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Cyanobenzaldehyde | HCID 66042 | — |
| Reactant | Dioxan ethanol | HCID 22560076 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71294558 | HCID 71294558 | — |
Reaction Steps
4-Cyanobenzaldehyde (3.0 g) was dissolved in a 1:1 mixed solution of ethanol/1,4-dioxane (80 mL), and bromoform (7.0 g) was added thereto under ice cooling. Subsequently, an ethanol solution (40 mL) of potassium hydroxide (7.6 g) was carefully added thereto, and the mixture was stirred for 6 hours at room temperature. After distilling off the solvent under reduced pressure, the residue thus obtained was diluted with water. The mixture was acidified with a 2 mol/L hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. After distilling off the solvent under reduced pressure, the residue was purified by silica gel column chromatography (50% to 100% ethyl acetate/hexane), and the title compound (2.6 g) was obtained as a crude product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096531B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-7378be704235403b91ef000e1dce154c |
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| Source note | uspto-grants-2015_08 |
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