HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25652Generated: October 28, 2026
2-(Ethylamino)ethanol → HCID 178464456, compound
https://huagongshe.com/reaction/25652
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Ethylamino)ethanol | HCID 8072 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178527576 | HCID 178527576 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178464456 | HCID 178464456 | 80.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06858651B2 |
|---|
| Source dataset | uspto-grants-2005_02 |
|---|
| ORD ID | ord-c5d1e7d215684b1bbcd3f8bd2d6edd61 |
|---|
| Source note | uspto-grants-2005_02 |
|---|