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
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 | 4-(1H-Pyrazol-1-yl)benzaldehyde | HCID 2776477 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | HCID 73990382 | HCID 73990382 | 89% |
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
| 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-c88fc07bbd0f48d6aca3c974b0f9287b |
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| Source note | uspto-grants-2002_10 |
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