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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787939Generated: October 28, 2026

Tert-butyl 4-hydroxypiperidine-1-carboxylate → Methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-(2-methoxyethoxy)benzoate

https://huagongshe.com/reaction/1787939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
ReactantHCID 23024267HCID 23024267—
ProductMethyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-(2-methoxyethoxy)benzoateHCID 6883257389.6%

Reaction Steps

Using a procedure similar to that of Example 26-B, methyl 2-hydroxy-4-(2-methoxyethoxy)benzoate (2.72 g, 12.02 mmol) is alkylated with 1-tert-butoxycarbonyl-4-hydroxy-piperidine (2.44 g, 12.02 mmol) to afford methyl 2-(1-tert-butoxycarbonylpiperidin-4-yloxy)-4-(2-methoxyethoxy)benzoate (4.41 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511066B2
Source datasetuspto-grants-2009_03
ORD IDord-ae2dc634d3044565838c9800d362b386
Source noteuspto-grants-2009_03