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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1460260Generated: November 2, 2026

Triethylamine → HCID 54029509, compound

https://huagongshe.com/reaction/1460260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
ReactantHCID 19983145HCID 19983145—
SolventDimethylformamideHCID 6228—
ProductHCID 54029509HCID 54029509—

Reaction Steps

A solution of 4.18 g (0.02 mole) of ethyl p-nitrophenylacetate in 200 mL of ethanol is subjected to catalytic hydrogenation. The mixture is filtered to remove the catalyst and the filtrate is concentrated to obtain quantitative yield of ethyl 4-aminophenylacetate. To an agitated solution of the ethyl 4-aminophenylacetate and 2.02 g (0.02 mole) of triethylamine in 50 ml of dimethylformamide is added dropwise a solution of 7.58 g (0.020 mole) of 1-(3-chloropropyl)-α,α-bis(4-fluorophenyl)-4-piperidinemethanol in 20 ml of dimethylformamide. After stirring at ambient temperature for 4 hr the reaction mixture is heated at 70° C. for 4 hr. The reaction mixture is concentrated and the crude product partitioned between methylene chloride and water. The methylene chloride solution is washed with water, dried over anhydrous magnesium sulfate, and concentrated to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05070087
Source datasetuspto-grants-1991_12
ORD IDord-ef97636c5c754503ba11e2054b38becd
Source noteuspto-grants-1991_12