HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856835Generated: October 30, 2026
Hydrochloric Acid → HCID 21862775, compound
https://huagongshe.com/reaction/856835
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-1-(4-fluorophenyl)ethan-1-one | HCID 96749 | — |
| Reactant | HCID 86754086 | HCID 86754086 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21862775 | HCID 21862775 | 17.1% |
Reaction Steps
4.68 g of the β-piperidinostyrene/diethyl phthalate mixture were dissolved in 70 ml of anhydrous tetrahydrofuran, and 1.01 g (10 mmol) of triethylamine were added to the resulting solution. 2.60 g (12 mmol) of 4-fluorophenacyl bromide were then added to the resulting mixture, which was then stirred at room temperature for 3 hours. At the end of this time, 30 ml of 1N aqueous hydrochloric acid were added to the reaction mixture, and the mixture was stirred at room temperature for a further 1 hour. It was then extracted with diethyl ether. The organic extract was washed with water and dried over anhydrous sodium sulfate. The solvent was then removed by distillation under reduced pressure and the residue was applied to a silica gel chromatography column and eluted with a 95:5 by volume mixture of hexane and ethyl acetate, to give 0.50 g of the title compound as a slightly yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | USRE039420E1 |
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| Source dataset | uspto-grants-2006_12 |
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| ORD ID | ord-306f56b6a7ca449392d3093c9bd73999 |
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| Source note | uspto-grants-2006_12 |
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