HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-{3-Aminobicyclo[1.1.1]pentan-1-yl}ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3-Aminobicyclo(1.1.1)pentane-1-carboxylic acid | HCID 25324661 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-{3-Aminobicyclo[1.1.1]pentan-1-yl}ethan-1-one | HCID 90410811 | — |
Reaction Steps
To a solution of 3-aminobicyclo[1.1.1]pentane-1-carboxylic acid (1 mmol) in anhydrous THF (2 mL) at 0° C. under nitrogen is added a methyllithium (1.4 M in diethyl ether, 4 mmol) in a dropwise manner. After addition, the reaction mixture is slowly allowed to warm to room temperature, stirred overnight, and treated with aqueous saturated ammonium chloride solution (4 mL). Ethyl acetate (2 mL) is added and organic layer are separated. The aqueous layer is extracted with ethyl acetate (3×1 mL). The combined organic layers are dried (Mg2SO4) and concentrated. The residue is purified by a flash chromatography on silica gel (EtOAc/hexnaes) to give 1-(3-aminobicyclo[1.1.1]pentan-1-yl)ethanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447025B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-d6d47c5580c947a994e003316c6043c0 |
| Source note | uspto-grants-2016_09 |