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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790402Generated: October 30, 2026

Triethylamine → 1-[1-(4-Cyanophenethyl)piperidin-4-yl]indoline

https://huagongshe.com/reaction/1790402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[1-(4-Hydroxyiminomethylphenethyl)piperidin-4-yl]indolineHCID 73861381—
SolventDichloromethaneHCID 6344—
Product1-[1-(4-Cyanophenethyl)piperidin-4-yl]indolineHCID 2203802628.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-a960bfee6eb84d98a502de7b889a1a4c
Source noteuspto-grants-2006_07