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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992936Generated: November 1, 2026

Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → HCID 73990353, compound

https://huagongshe.com/reaction/992936

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—
Reactant2-Fluoro-4-(1H-pyrazol-1-yl)benzaldehydeHCID 22631026—
SolventDichloromethaneHCID 6344—
SolventPotassium CarbonateHCID 11430—
ProductHCID 73990353HCID 7399035370%

Reaction Steps

A mixture of 2-fluoro-4-(1H-pyrazol-1-yl)benzaldehyde (1.06 g, 5.57 mmol, prepared as described in Reference Example 8), (1,3-dioxolan-2-ylmethyl)triphenylphosphonium bromide (3.60 g, 8.39 mmol), and TDA-1 (1.80 mL, 5.63 mmol) in dichloromethane (30 mL) and sat. aq. K2CO3 (30 mL) was heated to reflux for 20 h. The layers were separated and the aqueous layer was extracted with dichloromethane (2×15 mL). The combined organic layers were washed with water (30 mL) and brine (30 mL), dried (Na2SO4), and concentrated. THF (15 mL) and 10% HCl (15 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. Recrystallization from IPA provided 0.84 g (70%) of the title compound as tan needles. MS 217 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06472372B1
Source datasetuspto-grants-2002_10
ORD IDord-2fe7ed71f2d7445b8a115f2d4f2a1509
Source noteuspto-grants-2002_10