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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992941Generated: October 31, 2026

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → HCID 73990382, compound

https://huagongshe.com/reaction/992941

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—
Reactant4-(1H-Pyrazol-1-yl)benzaldehydeHCID 2776477—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
ProductHCID 73990382HCID 7399038289%

Reaction Steps

A mixture of 4-(1H-pyrazol-1-yl)-benzaldehyde (prepared as described in J. Med Chem. 1998, 41, 2390) (1.65 g, 9.58 mmol), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (6.45 g, 15.02 mmol), and TDA-1 (3.20 mL, 10.00 mmol) in dichloromethane (50 mL) and sat. aq. K2CO3 (50 mL) was heated to reflux for 20 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×25 mL). The combined organic layers were washed with water (50 mL) and brine (50 mL), dried (MgSO4), and concentrated. THF (25 mL) and 10% HCl (25 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, 3:1 hexane/ethyl acetate) provided 1.69 g (89%) of the title compound as a yellow solid. MS 199 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472372B1
Source datasetuspto-grants-2002_10
ORD IDord-c88fc07bbd0f48d6aca3c974b0f9287b
Source noteuspto-grants-2002_10