HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5501Generated: October 27, 2026
Sodium Chloride → N-1-Azabicyclo[2.2.2]oct-3-yl-2-chloroacetamide, monohydrochloride
https://huagongshe.com/reaction/5501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Quinuclidine, 3-amino-, dihydrochloride | HCID 197853 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-1-Azabicyclo[2.2.2]oct-3-yl-2-chloroacetamide, monohydrochloride | HCID 131716900 | 144% |
Reaction Steps
Potassium hydroxide (10 g) was added to a solution of 3-aminoquinuclidine dihydrochloride (10.45 g, 0.052 mole) in water (80 ml) saturated with sodium chloride. After stirring for 30 minutes, methylene chloride (75 ml) was added and the layers separated. The aqueous layer was washed with methylene chloride (2×75 ml), and the extracts combined with the methylene chloride layer above; dried over sodium sulfate, filtered, and the volume reduced to 100 ml. A solution of chloroacetyl chloride (3.11 g, 0.0273 mole) in methylene chloride (25 ml) was added dropwise and the mixture stirred overnight. The solvent was removed on a rotary evaporator. The residue was recrystallized from methanol-ethyl acetate to give a white solid (4.7 g), m.p. ca. 189°-195° C. The structure was confirmed by NMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05244899 |
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| Source dataset | uspto-grants-1993_09 |
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| ORD ID | ord-0036974a8e5f42138d995cc37559e5bb |
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| Source note | uspto-grants-1993_09 |
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