HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 346549Generated: October 27, 2026
Hydrochloric Acid → Ethyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate
https://huagongshe.com/reaction/346549
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | tert-Butyl 4-((4-(ethoxycarbonyl)-2-methoxyphenoxy)methyl)piperidine-1-carboxylate | HCID 21874806 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | Ethyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate | HCID 21874826 | 111.9% |
Reaction Steps
Formaldehyde (12M, 37% in water, 35 ml, 420 mmol) was added to a solution of ethyl 4-(1-(tert-butoxycarbonyl)piperidin-4-ylmethoxy)-3-methoxybenzoate (35 g, 89 mmol) in formic acid (35 ml). After stirring at 95° C. for 3 hours, the volatiles were removed by evaporation. The residue was dissolved in methylene chloride and 3M hydrogen chloride in ether (40 ml, 120 mmol) was added. After dilution with ether, the mixture was triturated until a solid was formed. The solid was collected by filtration, washed with ether and dried under vacuum overnight at 50° C. to give ethyl 3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (30.6 g, quant.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07173038B1 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-f3b46045d6aa4caeb0948e23860abc8e |
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| Source note | uspto-grants-2007_02 |
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