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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095444Generated: November 2, 2026

Ether hydrochloride → HCID 56829959, compound

https://huagongshe.com/reaction/2095444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEther hydrochlorideHCID 10953452—
ReactantHCID 59371348HCID 59371348—
SolventMethanolHCID 887—
ProductHCID 56829959HCID 56829959445.2%

Reaction Steps

To a solution of 1-(tert-butoxycarbonyl)-4-[2-(4-chlorobenzyloxy)ethyl]piperidine (760 mg, 0.47 mmol) in MeOH (0.5 mL) was added 2N anhydrous HCl/ether (1.5 mL, 3.0 mmol). The reaction mixture was stirred overnight, then evaporated, and the residue was dissolved in deionized water. EtOAc was used to wash the aqueous layer before the pH was altered to approx. 9-10. The aqueous layer was extracted three times with CH2Cl2, and the combined organic phases were dried over Na2SO4. After evaporation, 4-[2-(4-chlorobenzyloxy)ethyl]piperidine (531 mg, 97%) was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445684B2
Source datasetuspto-grants-2013_05
ORD IDord-b1b1094b90ee4ad4809e5c867674966e
Source noteuspto-grants-2013_05