HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → 2-(5-Amino-1,3,4-oxadiazol-2-yl)-1,1,1-trifluorobutan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Butanoic acid, 2-hydroxy-2-(trifluoromethyl)-, hydrazide | HCID 57729255 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(5-Amino-1,3,4-oxadiazol-2-yl)-1,1,1-trifluorobutan-2-ol | HCID 46942198 | — |
Reaction Steps
To hydrazide (34.07 g, 183 mmol) of step 2 in 275 mL of water was added KHCO3 (18.33 g, 183 mmol) followed by BrCN (19.39 g, 183 mmol) portionwise. After 3 h, the solid was filtered, washed with cold water and dried to afford the title compound. Additional compound could be recovered from the aqueous phase by extraction (ether-hexane, 1:1). 1H NMR (400 MHz, acetone-d6): δ 6.54 (s, 2H), 6.01 (s, 1H), 2.22 (m, 1H), 2.08 (m, 1H) and 0.99 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07553973B2 |
| Source dataset | uspto-grants-2009_06 |
| ORD ID | ord-b951095335714f0e81ea9d4706ed5ad4 |
| Source note | uspto-grants-2009_06 |