HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-[1-(4-Cyanophenethyl)piperidin-4-yl]indoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Trifluoroacetic anhydride | HCID 9845 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-[1-(4-Hydroxyiminomethylphenethyl)piperidin-4-yl]indoline | HCID 73861381 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[1-(4-Cyanophenethyl)piperidin-4-yl]indoline | HCID 22038026 | 28.9% |
Reaction Steps
1-[1-(4-Hydroxyiminomethylphenethyl)piperidin-4-yl]indoline (0.466 g) was dissolved in methylene chloride (6.5 ml) and triethylamine (0.35 ml) was added thereto. In a nitrogen atmosphere at −78° C., trifluoroacetic anhydride (0.14 ml) was added dropwise into the resultant solution followed by stirring for 3 hr. After adding a saturated aqueous solution of sodium bicarbonate, the resultant mixture was extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/methylene chloride/methanol system) to give the title compound (0.126 g) as a pale yellow oil (yield: 28.9%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07071201B2 |
| Source dataset | uspto-grants-2006_07 |
| ORD ID | ord-a960bfee6eb84d98a502de7b889a1a4c |
| Source note | uspto-grants-2006_07 |