HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430822Generated: October 30, 2026
Hydrochloric Acid → HCID 18352160, compound
https://huagongshe.com/reaction/430822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 18352164 | HCID 18352164 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18352160 | HCID 18352160 | — |
Reaction Steps
A 50 ml 3-necked round bottom flask was fitted with a pressure equalised dropping funnel, bubbler and magnetic stirrer. 8-(2,2-Difluoroethyl)-8-azabicyclo[3.2.1]octan-3-one (4.82 g, 25 mmol) was charged to the reaction flask and suspended in water (5 ml). Hydrochloric acid (5 ml, 5M) was added followed by solid ammonium chloride (2.23 g, 41 mmol) and the mixture stirred until the ammonium chloride had dissolved (5 minutes). The mixture was cooled to 5° C., a solution of potassium cyanide (5.03 g, 65 mmol) in water (7.5 ml) was added over 0.25 hour then the reaction was stirred at 0° C. for 3 hour. After this time, the lower oil phase was separated from the solid precipitate/aqueous phase to give 3-cyano-3-hydroxy-8-(2,2-difluoroethyl)-8-azabicyclo[3.2.1]octane as an oil which darkened on standing (5.32 g). The product was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323343B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-9eee111b3baa4ee1a6207aa3ff8d312c |
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| Source note | uspto-grants-2001_11 |
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