HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,1-Trifluorobutan-2-one → HCID 59774916, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,1-Trifluorobutan-2-one | HCID 238288 | — |
| Reactant | HCID 178419101 | HCID 178419101 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59774916 | HCID 59774916 | — |
Reaction Steps
To ethyl trifluoromethyl ketone (5.00 g, 40.0 mmol) in THF (20 ml) at room temperature was added 1-propynyl magnesium bromide (0.5 M in THF, 60 mL, 30.0 mmol). The reaction mixture was allowed to stand at rt 1 h, and concentrated in vacuo. The residue was partitioned between Et2O and aq. NH4OAc, the phases were separated, and the organic phase washed with brine, dried over MgSO4, filtered and concentrated (not to complete dryness), to afford a 50 wt. % solution (estimated by 1H NMR) of the title compound (remainder THF and Et2O), which was used without further purification. 1H NMR (400 MHz, DMSO-d6): 6.63 (s, 1H), 1.87 (s, 3H), 1.75-1.63 (m, 2H), 1.04 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960409B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-3e3017f1d3584f9489f4860cab98269c |
| Source note | uspto-grants-2011_06 |