HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 14373360, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 21278819 | HCID 21278819 | — |
| Product | HCID 14373360 | HCID 14373360 | — |
Reaction Steps
α-[(Nitro-1H-imidazol-1-yl)methyl]azabicyclo[3.1.0]hexane-6-ethanol from Example 4 was ring-opened by the action of 2-3 equivalents of hydrogen bromide in ethanol to produce the title compound as the hydrobromide salt, mp 204°-205° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04797397 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-60db5fd84ad443f9a385a12996f9f8d8 |
| Source note | uspto-grants-1989_01 |