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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251472Generated: October 27, 2026

2-Bromobenzoic acid → 1'-Benzyl-3H-spiro[isobenzofuran-1,4'-piperidin]-3-one

https://huagongshe.com/reaction/251472

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromobenzoic acidHCID 6940—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product1'-Benzyl-3H-spiro[isobenzofuran-1,4'-piperidin]-3-oneHCID 1026640620.5%

Reaction Steps

A solution of 2-bromobenzoic acid (20.12 g, 0.1 mol) in THF (200 mL) was treated dropwise with n-BuLi (2.5 M, 80 mL) at −78° C. The mixture was stirred at this temperature for 30 min, followed by dropwise addition of a solution of N-benzylpiperdine-4-one (26 g, 137 mmol) in THF (100 mL). The resulting mixture was stirred at −78° C. for 30 min, and was then allowed to warm to room temperature and stirred overnight. The reaction was quenched with water (100 mL) and the resulting mixture was washed with ether (100 mL). The aqueous layer was refluxed for 1 hr and then acidified to pH 2.5. The mixture was extracted with CHCl3 (3×50 mL), the combined organic layers were washed with brine, dried over Na2SO4 and concentrated to dryness to obtain 1′-benzyl-3H-spiro[isobenzofuran-1,4′-piperidin]-3-one 1b (6 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863449B2
Source datasetuspto-grants-2011_01
ORD IDord-eafacdc9da374da4b97e44dc82c3b064
Source noteuspto-grants-2011_01