HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → tert-Butyl 2-((2,2,2-trifluoroethyl)carbamoyl)hydrazinecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | tert-Butyl carbazate | HCID 70091 | — |
| Reactant | 1,1,1-Trifluoro-2-isocyanatoethane | HCID 10678231 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | tert-Butyl 2-((2,2,2-trifluoroethyl)carbamoyl)hydrazinecarboxylate | HCID 86722559 | 79% |
Reaction Steps
To a stirred solution of tert-butyl hydrazinecarboxylate (1.0 g, 8 mmol) in anhydrous benzene (10.0 mL) was added 1,1,1-trifluoro-2-isocyanatoethane (1.06 g, 8 mmol) neat via syringe to give a gelatin like mixture. Anhydrous THF was added to give a clear solution which was stirred for 10 minutes, after which time the reaction mixture was evaporated to afford the title compound as a white solid (1.62 g, 79%): 1H NMR (400 MHz, CDCl3) δ 6.63 (s, 1H), 6.40 (d, J=2.2 Hz, 1H), 5.84 (s, 1H), 3.88 (qd, J=9.0, 6.6 Hz, 2H), 1.48 (s, 9H); 19F NMR (376 MHz, CDCl3) δ −73.20. This material is used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09215870B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-70c3e75d93a54be499f363250a8c821a |
| Source note | uspto-grants-2015_12 |