HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992937Generated: October 31, 2026
Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- → HCID 73990347, compound
https://huagongshe.com/reaction/992937
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanamine, 2-(2-methoxyethoxy)-N,N-bis[2-(2-methoxyethoxy)ethyl]- | HCID 112414 | — |
| Reactant | (1,3-Dioxolan-2-ylmethyl)triphenylphosphonium bromide | HCID 2724194 | — |
| Reactant | 3-Methoxy-4-(1H-pyrazol-1-yl)benzaldehyde | HCID 22631004 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 73990347 | HCID 73990347 | 86% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06472372B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-e6adbec3b0fb4209913f8802a33c3912 |
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| Source note | uspto-grants-2002_10 |
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