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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390138Generated: October 30, 2026

7-bromo-2',3'-dihydro-1'H-spiro[isoindoline-1,4'-pyridin]-3-one → 7-Bromospiro[isoindoline-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/390138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-bromo-2',3'-dihydro-1'H-spiro[isoindoline-1,4'-pyridin]-3-oneHCID 58295744—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
Product7-Bromospiro[isoindoline-1,4'-piperidin]-3-oneHCID 58295726100%

Reaction Steps

A solution of 7-bromo-2′,3′-dihydro-1′H-spiro[isoindoline-1,4′-pyridin]-3-one (2 g, 0.0072 mol) in CH3COOH was hydrogenated in the presence of PtO2 for 1.5 h. The catalyst was removed by filtration and the filtrate was concentrated to give the crude product which was washed with saturated aq Na2CO3. The solvent was removed to give the 7-bromospiro[isoindoline-1,4′-piperidin]-3-one (2 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383629B2
Source datasetuspto-grants-2013_02
ORD IDord-fa458ef465bd4795b4d1554c03548242
Source noteuspto-grants-2013_02