HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → HCID 67390371, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Phenylmethyl N-[1-[5-(trifluoromethyl)-1,2,4-oxadiazol-3-yl]cyclopropyl]carbamate | HCID 58431168 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 67390371 | HCID 67390371 | — |
Reaction Steps
[1-(5-Trifluoromethyl-1,2,4-oxadiazol-3-yl)-cyclopropyl]-carbamic acid benzyl ester (0.22 g, 0.67 mmol) was dissolved in 33% HBr in acetic acid (0.5 mL) and the reaction allowed to stir for 30 min at RT. The mixture was diluted with Et2O resulting is formation of a white precipitate. The majority of the liquid was decanted off and the residue concentrated under reduce pressure to give 1-(5-trifluoromethyl-1,2,4-oxadiazol-3-yl)-cyclopropylamine hydrobromide (0.19 g, 0.69 mmol) as an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552205B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-3b90b03dad954bc28afbde542ef15ae3 |
| Source note | uspto-grants-2013_10 |