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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472983Generated: October 30, 2026

Sodium hydride → HCID 58197381, compound

https://huagongshe.com/reaction/472983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant1-Indanone, 6-bromo-HCID 139778—
ReactantHCID 58197660HCID 58197660—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58197381HCID 5819738146%

Reaction Steps

To a solution of 2-(2-bromoethyl)-1-(bromomethyl)-3,4-difluorobenzene (3 g, 9.62 mmol) and 6-bromo-2,3-dihydro-1H-inden-1-one (2.03 mg, 9.62 mmol) in THF (20 mL) was added NaH (0.58 mg, 14.43 mmol), and the mixture was refluxed for 2 hour. The reaction was cooled and quenched with ice-water. The mixture was extracted with EtOAc. The organic layer was washed with brine, dried over Na2SO4, filtered and concentrated to give the residue, which was purified by preparative TLC to afford 6-bromo-5′,6′-difluoro-3′,4′-dihydro-1′H-spiro[indene-2,2′-naphthalen]-1(3H)-one (1.6 g, 46%). 1H NMR (CDCl3): 1.68 (m, 1H), 2.01 (m, 1H), 2.47 (d, 1H), 2.72 (m, 2H), 2.89 (d, 1H), 3.07 (m, 2H), 6.71 (m, 1H), 6.86 (m, 1H), 7.22 (d, 1H), 7.63 (d, 1H), 7.92 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633212B2
Source datasetuspto-grants-2014_01
ORD IDord-e7319b5bd7f84b8580fbc73426453f60
Source noteuspto-grants-2014_01