HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364314Generated: November 1, 2026
Hydrochloric Acid → HCID 178456094, compound
https://huagongshe.com/reaction/1364314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 66935237 | HCID 66935237 | — |
| Catalyst | Zinc bromide | HCID 10421208 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178456094 | HCID 178456094 | 58.9% |
Reaction Steps
To N-benzyloxycarbonyl-(1R)-1-cyanopropylamine (85.6 mg) in suspension (3 ml), sodium azide (28 mg) and zinc bromide (88.3 mg) were added and the mixture was stirred under heating and reflux for 24 hours. 3N hydrochloric acid and ethyl acetate were added to the reaction solution and the mixture was stirred until there were no longer any insolubles. The obtained solution was extracted with ethyl acetate, then the organic layer was concentrated. 0.25N sodium hydroxide aqueous solution was added to the residue, the mixture was stirred for 30 minutes, and the insoluble compound was filtered. 6N hydrochloric acid was added to the filtrate to adjust to pH 1, then this was concentrated. The residue was diluted with 1N hydrochloric acid, then the solids were collected by filtration to obtain the title compound (60.4 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888348B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-48a33bda341a42c18649c3f49f56b1bc |
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| Source note | uspto-grants-2011_02 |
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