Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182721Generated: October 31, 2026

Hydrochloric Acid → HCID 66783848, compound

https://huagongshe.com/reaction/1182721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBoraneHCID 6331—
ReactantSodium HydroxideHCID 14798—
Reactant5-Fluoro-3h-spiro[isobenzofuran-1,4'-piperidin]-3-oneHCID 22660731—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66783848HCID 6678384855.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 5-fluoro-3H-spiro[2-benzofuran-1,4′-piperidin]-3-one (420 mg, 1.9 mmol) in tetrahydrofuran (4.2 ml) was added dropwise a 1M borane solution in tetrahydrofuran (3.8 ml, 3.8 mmol) at 0° C. The mixture was refluxed overnight and then cooled to 0° C. HCl 5 N (2 ml) was added dropwise. The mixture was refluxed for 5 hours, cooled to 0° C., diluted with water and basified with NaOH 5 N (pH 10). The mixture was extracted 3 times with ethyl acetate. The combined extracts were dried over Na2SO4, filtered and concentrated in vacuo. The residue was stirred with ether and filtrated. The filtrate was concentrated in vacuo to provide 0.22 g (55%) of 5-fluoro-3H-spiro[2-benzofuran-1,4′-piperidine] as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08664216B2
Source datasetuspto-grants-2014_03
ORD IDord-e873bf3c1ab04fd1b19d87663f1703ad
Source noteuspto-grants-2014_03