HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 117839689, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 5-(trifluoroMethyl)thiophene-2-carbaldehyde | HCID 72213188 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 117839689 | HCID 117839689 | — |
Reaction Steps
To a tetrahydrofuran solution (2.0 mL) of 5-(trifluoromethyl)thiophene-2-carbaldehyde (80.0 mg, 0.444 mmol), methylmagnesium bromide (533 μL, 0.444 mmol) was added at 0° C. and the resultant mixture was stirred at room temperature for 5 minutes. After completion of the reaction, acetic acid was added to the reaction solution and the resultant mixture was concentrated under reduced pressure. To the obtained residue, water was added and extraction from the resultant mixture with ethyl acetate was performed. The organic layer was concentrated under reduced pressure to obtain a crude product of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403798B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-8ae626faf95d45f8896018a2f33769ad |
| Source note | uspto-grants-2016_08 |