HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889037Generated: October 31, 2026
HCID 2775915, compound → HCID 53215517, compound
https://huagongshe.com/reaction/889037
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 2775915 | HCID 2775915 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53215517 | HCID 53215517 | — |
Reaction Steps
5-Oxo-1-(3-trifluoromethyl-phenyl)-pyrrolidine-3-carboxylic acid (0.35 g, 1.28 mmol) in diethyl ether (5 ml) was added to a solution of lithium aluminium hydride (0.097 g, 2.56 mmol) in THF (5 ml) at temperature 0° C. over a period of 10 min. The mixture was refluxed for 2 hours and then stirred at room temperature for 20 hours. The reaction mixture was diluted with diethyl ether (15 ml) and quenched with water (10 ml). The organic layer was separated and aqueous layer was extracted with diethyl ether. The combined organic layer was washed with saturated brine solution, dried over Na2SO4 and evaporated to obtain a residue which was purified by preparative TLC to afford [1-(3-trifluoromethyl-phenyl)-pyrrolidin-3-yl]-methanol as a colorless mass (0.2 g, 64%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08252797B2 |
|---|
| Source dataset | uspto-grants-2012_08 |
|---|
| ORD ID | ord-8a9de5f121b94039bcf782dc96bbb67a |
|---|
| Source note | uspto-grants-2012_08 |
|---|