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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Tert-butoxycarbonyl-4-(3-methanesulfonyloxypropoxy)piperidine | HCID 22494665 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-(3-methoxypropyloxy)-N-t-butyloxycarbonylpiperidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884868B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-1ddfa5733be44a64b3fcbd4f7d1b98ae |
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| Source note | uspto-grants-2005_04 |
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