HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289255Generated: October 30, 2026
Ammonium Chloride → HCID 178451026, compound
https://huagongshe.com/reaction/1289255
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Reactant | HCID 10687030 | HCID 10687030 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178451026 | HCID 178451026 | 84.3% |
Reaction Steps
A mixture of tert-butyl (4R)-4-(benzyloxycarbonylamino)-4-cyanobutyrate (1.53 g, 4.8 mmol), ammonium chloride (0.28 g, 5.2 mmol), sodium azide (0.345 g, 5.3 mmol) and dry DMF (6 ml) was stirred and heated at 90°-95° C. under argon for 20 hours. The mixture was cooled and concentrated and the residue partitioned between ice-cooled water (40 ml) and ethyl acetate (30 ml) with the pH of the aqueous phase being adjusted to 3 by the addition of 10% aqueous citric acid solution (ca. 10 ml). The aqueous layer was extracted with further ethyl acetate (3×30 ml) and the combined organic solution washed with water (4×25 ml), dried (MgSO4) and evaporated. A solution of the residue in dichloromethane (3 ml) was added dropwise to stirred hexane (20 ml) and the precipitate was collected, washed with hexane and dried to give tert-butyl (4R)-4-(benzyloxycarbonylamino)-4-(tetrazol-5-yl)butyrate (1.462 g, 84%), m.p. 99°-101° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05747499 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-166d4feeb7d8485898e6ac3840d5025d |
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| Source note | uspto-grants-1998_05 |
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