HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → C-(5-(3-fluorophenoxy)thiophen-2-yl)methylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5-(3-Fluorophenoxy)thiophene-2-carbonitrile | HCID 23130613 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | C-(5-(3-fluorophenoxy)thiophen-2-yl)methylamine | HCID 23130606 | 80.7% |
Reaction Steps
To a solution of 5-(3-fluorophenoxy)thiophene-2-carbonitrile described in Preparation Example 22 (670 mg, 3 mmol) in tetrahydrofuran (30 mL) was added lithium aluminum hydride (460 mg, 12 mmol), and the solution was stirred at room temperature for 16 hours. Water and ethyl acetate were added to the reaction solution, which was then partitioned, the organic layer was filtered with NH silica gel, the filtrate was evaporated in vacuo, and the title compound (570 mg, 2.42 mmol, 80.7%) was obtained as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07932272B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-efebfa5e8509454b8eb7421c76feefbe |
| Source note | uspto-grants-2011_04 |