HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13288028, compound → HCID 12804791, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13288028 | HCID 13288028 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 12804791 | HCID 12804791 | — |
Reaction Steps
A solution of 5.90 g of 1-formyl-3-hydroxy-3-(α-phenyl-2-tolyl)pyrrolidine in 60 ml of dry THF is added dropwise to a suspension of 3 g of LiAlH in 30 ml of dry THF and the mixture is refluxed for 4 hours. After cooling the mixture is separated and the residue extracted with ether. The combined organic solution is dried (Na2SO4) and concentrated to an oil. This oil is dissolved in 100 ml of hexane and after cooling 16 hours the product is isolated by filtration to provide 3-hydroxy-1-methyl-3-(α-phenyl-2-tolyl)pyrrolidine, mp 108°-109° C. Dilution of the mother liquor with 50 ml of hexane gives a second crop of 3-hydroxy-1-methyl-3-(α-phenyl-2-tolyl)pyrrolidine, mp 107°-108° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04414219 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-d5661b3cbb0647448364eee392a5bfe5 |
| Source note | uspto-grants-1983_11 |