HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Nitrobenzyl)pyrrolidine → 4-(Pyrrolidin-1-ylmethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Nitrobenzyl)pyrrolidine | HCID 783522 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(Pyrrolidin-1-ylmethyl)aniline | HCID 776852 | 36.9% |
Reaction Steps
To a solution of 1-(4-nitro-benzyl)-pyrrolidine (1.37 g) in ethanol (66 mL) tin(II)-chloride dihydrate (9.0 g) was added portionwise and the resulting mixture refluxed for 2 h. The reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution, the aqueous phase extracted with additional ethyl acetate, the combined organic phases dried (Na2SO4) and evaporated, which gave, after chromatography on silica using dichloromethane/methanol, the title compound (432 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07504410B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-c3995c5ded094789b555339d723dd692 |
| Source note | uspto-grants-2009_03 |