Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630402Generated: October 30, 2026

Triethylamine → HCID 178484575, compound

https://huagongshe.com/reaction/630402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromoethanolHCID 10898—
ReactantEthanol, 1-bromo-HCID 14202443—
ReactantHCID 178484861HCID 178484861—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178484575HCID 17848457576%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of trans-4-(methylamino)cyclohexyl hydroxy(di-2-thienyl)acetate (intermediate 5; 300 mg; 0.85 mmol), 2-bromoethanol (0.145 ml; 2.05 mmol) and triethylamine (0.36 ml; 2.58 mmol) in 4.5 ml of acetonitrile and 3.5 ml of THF was stirred at 80° C. in a sealed vessel for 16 hr. Additional amounts of bromoethanol (0.145 ml; 2.05 mmol), triethylamine (0.36 ml; 2.58 mmol), acetonitrile (3.5 ml) and THF (3.5 ml) were added and the stirring and heating prosecuted for 24 additional hours. The solution was evaporated to dryness, dissolved in dichloromethane, washed with brine, dried and concentrated. Purification by preparative reversed-phase HPLC (Cl3CH/MeOH from 1:0 to 9:1) gave 76% of the title product as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315463B2
Source datasetuspto-grants-2016_04
ORD IDord-45f3946e87604b64b18545a6efa41cf4
Source noteuspto-grants-2016_04