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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827552Generated: October 29, 2026

Triethylamine → HCID 85955915, compound

https://huagongshe.com/reaction/1827552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclohexanecarbonyl chlorideHCID 75938—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(2-(Pyrrolidin-1-yl)ethoxy)anilineHCID 6493749—
SolventDichloromethaneHCID 6344—
ProductHCID 85955915HCID 85955915—

Reaction Steps

To a solution of 4-(2-pyrrolidin-1-yl-ethoxy)-phenylamine (2.15 g, 10.42 mmol) and triethylamine (3.27 mL, 23.4 mmol) in 100 mL methylene chloride at 0° C. was added cyclohexanecarbonyl chloride (1.46 mL, 10.94 mmol), dropwise. The reaction mixture was stirred at room temperature for 24 hr. Saturated aqueous sodium bicarbonate was added and the layers were separated. The aqueous layer was washed with 50 mL methylene chloride. The combined organic layers were dried (magnesium sulfate), filtered, and concentrated to afford the title compound of Step A. MS 317.2 (M+1)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053212B2
Source datasetuspto-grants-2006_05
ORD IDord-9f6d95030f714bef94c8a05f8622c746
Source noteuspto-grants-2006_05