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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromobenzoic acid | HCID 6940 | — |
| Reactant | 1-Benzyl-4-piperidone | HCID 19220 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1'-Benzyl-3H-spiro[isobenzofuran-1,4'-piperidin]-3-one | HCID 10266406 | 20.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863449B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-eafacdc9da374da4b97e44dc82c3b064 |
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| Source note | uspto-grants-2011_01 |
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