HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(2-Anilinoethyl)-4-methoxymethoxypiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 1-(Anilinocarbonylmethyl)-4-methoxymethoxypiperidine | HCID 22923688 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(2-Anilinoethyl)-4-methoxymethoxypiperidine | HCID 22923706 | 98.6% |
Reaction Steps
A solution of 3.64 g of 1-(anilinocarbonylmethyl)-4-methoxymethoxypiperidine in 10 ml of tetrahydrofuran was added to a suspension of 630 mg of lithium aluminum hydride in 50 ml of tetrahydrofuran. The mixture was refluxed for 3 hours. To the reaction mixture were added 1.5 ml of an aqueous solution containing 10% of potassium hydroxide and 1.5 ml of water. The mixture was diluted with ethyl acetate, and the dilution was filtered. The solvent in the filtrate was removed by distillation to obtain 3.41 g of 1-(2-anilinoethyl)-4-methoxymethoxypiperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05506239 |
| Source dataset | uspto-grants-1996_04 |
| ORD ID | ord-c3ad9d8cfb27477b9f7d01af74960ffe |
| Source note | uspto-grants-1996_04 |