HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767729Generated: October 31, 2026
Hydrochloric Acid → Ethyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate
https://huagongshe.com/reaction/1767729
Participants
| Role | Name | HCID | Charge |
|---|
| 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 | — |
| Solvent | Water | HCID 962 | — |
| Product | Ethyl 3-methoxy-4-((1-methylpiperidin-4-yl)methoxy)benzoate | HCID 21874826 | 111.9% |
Reaction Steps
Formaldehyde (35 ml of a 37% solution in water, 420 mmol) was added to a solution of ethyl 3-methoxy-4-(1-tert-butyloxycarbonylpiperidin-4-ylmethoxy)benzoate (35 g, 89 mmol) in formic acid (35 ml) and the reaction was heated at 95° C. for 3 hours. The reaction was cooled, the volatiles we removed in vacuo and the residue was dissolved in dichloromethane. 3.0 N Hydrogen chloride in diethyl ether (40 ml, 120 mmol) was added, together with a little diethyl ether and a solid was precipitated. Collection of the solid by suction filtration followed by drying in vacuo yielded ethyl 3-methoxy-4-(1-methylpiperidin-4-ylmethoxy)benzoate (30.6 g, 100% yield) as a white solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07235559B1 |
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| Source dataset | uspto-grants-2007_06 |
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| ORD ID | ord-b51fef20406d493abec03084bf35be17 |
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| Source note | uspto-grants-2007_06 |
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