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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25652Generated: October 28, 2026

2-(Ethylamino)ethanol → HCID 178464456, compound

https://huagongshe.com/reaction/25652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Ethylamino)ethanolHCID 8072—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178527576HCID 178527576—
SolventEthanolHCID 702—
ProductHCID 178464456HCID 17846445680.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 2.4 mg (5.26 mmol) of trans-N-[4-(5-Bromo-pentyl)-cyclohexyl]-4-trifluoromethyl-benzenesulfonamide in 36 ml of EtOH was treated with 2.1 ml (21.53 mmol) of ethyl-(2-hydroxy-ethyl)-amine, 1.8 g (21.43 mmol) of NaHCO3 and stirred over night at 90° C. The reaction cooled, filtered, evaporated and the residue extracted with aqueous saturated NaHCO3/EtOAc (3×). The organic phases were washed with aqueous 10% NaCl, dried (Na2SO4), filtered and evaporated. Purification by flash column chromatography on silica gel (EtOAc/EtOH/NH3 25% 98:2:1) gave 1.96 g (80%) of trans-N-(4-{5-[Ethyl-(2-hydroxy-ethyl)-amino]-pentyl}-cyclohexyl)-4-trifluoromethyl-benzenesulfonamide, MS: 463 (M−H−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858651B2
Source datasetuspto-grants-2005_02
ORD IDord-c5d1e7d215684b1bbcd3f8bd2d6edd61
Source noteuspto-grants-2005_02