HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095003Generated: October 31, 2026
Piperidine → Ethyl 3,4-bis(2-methoxyethoxy)benzoate
https://huagongshe.com/reaction/1095003
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 3,4-Dihydroxybenzoate | HCID 77547 | — |
| Reactant | 2-Amino-5-piperidin-1-yl-benzoic acid ethyl ester | HCID 61306567 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Ethyl 3,4-bis(2-methoxyethoxy)benzoate | HCID 2808992 | 93% |
Reaction Steps
3,4-Dihydroxy-benzoic acid ethyl ester (compound A′) (2.0 g) was dissolved in acetone (20 ml). Potassium carbonate (4.3 g) and 1-bromo-2-methoxy-ethane (compound D) (5 ml) were added to the solution at room temperature, and the mixture was then stirred at 70° C. for 24 hr. After the completion of the reaction, the reaction solution was allowed to stand for cooling at room temperature, and the reaction system was concentrated under the reduced pressure. Distilled water was added to the residue, and the mixture was then subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated under the reduced pressure. The residue was purified by column chromatography using a hexane-acetone system to give 3,4-bis-(2-methoxy-ethoxy)-benzoic acid ethyl ester (3.06 g, yield 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08134015B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c7a9a14c1a3f443d9414d55c47afcadd |
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| Source note | uspto-grants-2012_03 |
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