HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → 2-[1-[2-(Tert-butyldiphenylsiloxy)ethyl]cyclohexyl]ethylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | N-[2-[1-[2-(tert-Butyldiphenylsiloxy)ethyl]cyclohexyl]ethyl]-phthalimide | HCID 59714868 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[1-[2-(Tert-butyldiphenylsiloxy)ethyl]cyclohexyl]ethylamine | HCID 59714973 | 104% |
Reaction Steps
To a solution of N-[2-[1-[2(tert-butyldiphenylsiloxy)ethyl]cyclohexyl]-ethyl]phthalimide (1.52 g) dissolved in ethanol (30 mL) was added hydrazine monohydrate. The reaction solution was heated under reflux for 4 hours. To this was added diethyl ether and the insolbles were filtered off. The solvent was then distilled off under reduced pressure. To this was added chloroform, and the solution was made basic by addition of a 1N aqueous hydroxide solution. The solution was then extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, filtered, and then, the solvent was distilled off under reduced pressure to give the title compound (1.20 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07375115B2 |
| Source dataset | uspto-grants-2008_05 |
| ORD ID | ord-e31492b101284082967088fa9d8667a3 |
| Source note | uspto-grants-2008_05 |