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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 559340Generated: October 26, 2026

(S)-6-benzyl-6-aza-spiro[2,5]octan-4-ol → (4S)-6-Azaspiro[2.5]octan-4-ol

https://huagongshe.com/reaction/559340

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-6-benzyl-6-aza-spiro[2,5]octan-4-olHCID 25204267—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product(4S)-6-Azaspiro[2.5]octan-4-olHCID 44541813—

Reaction Steps

100 mg (S)-6-benzyl-6-aza-spiro[2.5]octan-4-ol were dissolved in 1 ml methanol and hydrogenated over palladium on barium sulfate. After de-benzylation (IPC by GC), the catalyst was filtered and the filtrate was concentrated under reduced pressure to provide the title compound. The hydrochloride salt of the title compound can be obtained by treating the aminoalcohol with HCl in ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063042B2
Source datasetuspto-grants-2011_11
ORD IDord-bea54a87230f4886bf0b03b93d767af7
Source noteuspto-grants-2011_11