Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166103Generated: November 1, 2026

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → HCID 73990347, compound

https://huagongshe.com/reaction/1166103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]-HCID 112414—
Reactant(1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromideHCID 2724194—
Reactant3-Methoxy-4-(1H-pyrazol-1-YL)benzaldehydeHCID 22631004—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
ProductHCID 73990347HCID 7399034786%

Reaction Steps

A mixture of 3-methoxy-4-(1H-pyrazol-1-yl)benzaldehyde (1.52 g, 7.52 mmol, prepared as described in Reference Example 5), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (4.85 g, 11.30 mmol), and TDA-1 (2.40 mL, 7.50 mmol) in dichloromethane (35 mL) and sat. aq. K2CO3 (35 mL) was heated to reflux for 18 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 (MgSO4), and concentrated. THF (20 mL) and 10% HCl (20 mL) were added and the mixture was stirred for 1 h at rt. The reaction mixture was cooled to 0° C., made basic with 10% NaOH, and extracted with ethyl acetate (3×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. Purification by chromatography (SiO2, 2:1 hexane/ethyl acetate) provided 1.47 g (86%) of the title compound as a yellow solid. MS 229 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613747B2
Source datasetuspto-grants-2003_09
ORD IDord-76a7e0df9946439b9f183dd894a60dfd
Source noteuspto-grants-2003_09