HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639723Generated: October 30, 2026
Hydrochloric Acid → HCID 11593499, compound
https://huagongshe.com/reaction/639723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromo-beta,beta-difluorostyrene | HCID 11356427 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11593499 | HCID 11593499 | 24.5% |
Reaction Steps
To a mixture of 0.67 g of magnesium and 10 ml of tetrahydrofuran was added a catalytic amount of iodine, and added dropwise a solution of 6.0 g of 1-bromo-3-(2,2-difluoroethenyl)benzene in 20 ml of tetrahydrofuran at 55° C. After stirred at room temperature for 15 minutes, a solution of 3.98 g of 1-formylpiperidine in 5 ml of tetrahydrofuran was added dropwise. This was heated under reflux for 15 minutes, and ice water and 10% hydrochloric acid were added, followed by extraction with t-butyl methyl ether. The organic layer washed with an aqueous saturated sodium chloride solution, dried over anhydrous magnesium sulfate and then concentrated. The resulting residue was subjected to silica gel column chromatography to obtained 1.13 g of oily 3-(2,2-difluoroethenyl)benzaldehyde [Compound No. (l)].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07691883B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-6ad25b865a9f412390025343bdd47b06 |
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| Source note | uspto-grants-2010_04 |
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