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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2416461Generated: October 25, 2026

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → (2E)-3-(6-Quinoxalinyl)-2-propenal

https://huagongshe.com/reaction/2416461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
ReactantQuinoxaline-6-carboxaldehydeHCID 763958—
Reactant(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromideHCID 2724194—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
Product(2E)-3-(6-Quinoxalinyl)-2-propenalHCID 2263079965.1%

Reaction Steps

A mixture of 6-quinoxalinecarboxaldehyde (0.62 g, 3.92 mmol, prepared as described in Photochem. Photobiol. 1991, 54, 7), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (2.50 g, 5.82 mmol), and TDA-1 (1.20 mL, 3.75 mmol) in dichloromethane (20 mL) and sat. aq. K2CO3 (20 mL) was heated to reflux for 4 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×20 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (Na2SO4), and concentrated. THF (10 mL) and 10% HCl (10 mL) were added and the mixture was stirred for 1 h at rt. The mixture was cooled to 0° C., the precipitated solids were removed by filtration, washed with water and dried in vacuo to give 0.47 g (65%) of the title compound as a tan solid. MS 185 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06825170B2
Source datasetuspto-grants-2004_11
ORD IDord-fa7621ee5e6a4b3ca751b1503d33c589
Source noteuspto-grants-2004_11