HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannous Chloride → cis-(6-Benzhydryl-tetrahydropyran-3-yl)-(4-amino-benzyl)-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | Cis-(6-benzhydryl-tetrahydropyran-3-yl)-(4-nitro-benzyl)-amine | HCID 11531477 | — |
| Reactant | Ethyl acetate triethylamine | HCID 22036596 | — |
| Solvent | Ethanol ethylacetate | HCID 21584252 | — |
| Product | cis-(6-Benzhydryl-tetrahydropyran-3-yl)-(4-amino-benzyl)-amine | HCID 11510954 | 60% |
Reaction Steps
A mixture of cis-(6-benzhydryl-tetrahydropyran-3-yl)-(4-nitro-benzyl)-amine (16f) (0.16 g, 0.39 mmol) and SnCl2/2H2O (0.35 g, 1.55 mmol) in EtOH/EtOAc (20 ml, 7:3) was heated to reflux for 1.5 h (monitored by TLC, Hex/EtOAc/Et3N 5:5:0.4). After removal of the solvent, the residue was diluted with 10% NaHCO3 and EtOAc and stirred vigorously for 30 min. After filtration the organic phase was separated and the aqueous phase was extracted with EtOAc (20 ml×2). The combined organic phase was dried over Na2SO4. After removal of the solvent, flash chromatography gave 16o, cis-(6-benzhydryl-tetrahydropyran-3-yl)-(4-amino-benzyl)-amine (0.087 g, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08937189B2 |
| Source dataset | uspto-grants-2015_01 |
| ORD ID | ord-34dce869c474405dbc15cfe507bd8e7b |
| Source note | uspto-grants-2015_01 |