HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 5-Aminomethyl-2-(3-dipropylaminobutyl)-1-methoxymethoxy-indane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium sodium tartarate | HCID 9855836 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5-Cyano-2-(3-dipropylaminobutyl)-1-methoxymethoxy-indane | HCID 23079297 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Aminomethyl-2-(3-dipropylaminobutyl)-1-methoxymethoxy-indane | HCID 23079303 | 42.9% |
Reaction Steps
The compound (436.8 mg) obtained in Example 127-9 was dissolved in THF (21.8 ml) and added with lithium aluminum hydride (138.7 mg), followed by stirring at room temperature for 24 hours. The reaction solution was added with ethyl acetate, methanol, and a 10% aqueous potassium sodium tartrate solution, and stirred for 1 hour, followed by separation/extraction with chloroform. The extract was washed with saturated saline solution and dried with anhydrous sodium sulfate, followed by concentration under reduced pressure. The residue was purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (189.7 mg) as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07176227B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-591a03f846a04a1cb07ce7486f941b12 |
| Source note | uspto-grants-2007_02 |