HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → N-[2-(4-(2-Hydroxyethoxy)-phenyl)-1-methylethyl]-2-(6-chloro-pyridin-2-yl)-morpholine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | N-[2-(4-(2-Hydroxyethoxy)-phenyl)-1-methylethyl]-2-(6-chloro-pyridin-2-yl)-morpholin-5-one | HCID 14578858 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Borane;tetrahydrofuran | HCID 2723981 | — |
| Product | N-[2-(4-(2-Hydroxyethoxy)-phenyl)-1-methylethyl]-2-(6-chloro-pyridin-2-yl)-morpholine | HCID 14578859 | — |
Reaction Steps
0.7 g of N-[2-(4-(2-hydroxyethoxy)-phenyl)-1-methylethyl]-2-(6-chloro-pyridin-2-yl)-morpholin-5-one are dissolved in 20 ml of tetrahydrofuran and over a period of 3 hours at ambient temperature 3 times 4 ml of a 1 molar borane/tetrahydrofuran solution are added. Then 30 ml of acetone are added and the mixture is evaporated down. The residue is dissolved in 100 ml of methanol and stirred for 20 hours. The solvent is distilled off in vacuo and the residue is purified over a silica gel column with ethyl acetate as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05026702 |
| Source dataset | uspto-grants-1991_06 |
| ORD ID | ord-13cc385a9b754e6ebb0fcb5c7d46d581 |
| Source note | uspto-grants-1991_06 |