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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816715Generated: November 2, 2026

1-Tert-butoxycarbonyl-4-(3-methanesulfonyloxypropoxy)piperidine → 4-(3-methoxypropyloxy)-N-t-butyloxycarbonylpiperidine

https://huagongshe.com/reaction/1816715

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Tert-butoxycarbonyl-4-(3-methanesulfonyloxypropoxy)piperidineHCID 22494665—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
Product4-(3-methoxypropyloxy)-N-t-butyloxycarbonylpiperidineHCID 22494667—

Reaction Steps

To a solution of 4-[3-(methanesulfonyloxy)propyloxy]-N-t-butyloxycarbonylpiperidine (3.76 g) in methanol (20 ml) was added 28% sodium methoxide methanol solution (22.7 ml), and the mixture was stirred under refluxing for 1.5 hours. The reaction mixture was evaporated in vacuo and dissolved in ethyl acetate (200 ml). The solution was washed twice with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo. The resulting residue was chromatographed on silica gel (200 ml) eluting with a mixture of n-hexane and ethyl acetate (2:1 v/v). The fractions containing the object compound were collected and evaporated under reduced pressure to give 4-(3-methoxypropyloxy)-N-t-butyloxycarbonylpiperidine (2.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884868B1
Source datasetuspto-grants-2005_04
ORD IDord-1ddfa5733be44a64b3fcbd4f7d1b98ae
Source noteuspto-grants-2005_04