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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656368Generated: October 29, 2026

Benzyl Bromide → HCID 18449405, compound

https://huagongshe.com/reaction/656368

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 18449403HCID 18449403—
SolventDimethylformamideHCID 6228—
ProductHCID 18449405HCID 18449405—

Reaction Steps

To a solution of (±)-1-(4-methoxybenzyl)-5′-nitro-spiro[imidazolidine-4,2′-indane]-2,5-dione from Step A (165 mg, 0.45 mmol) in DMF (1 mL) was added sodium hydride (18 mg of a 60% dispersion in mineral oil, 0.45 mmol). The mixture was stirred for 5 min at ambient temperature and benzyl bromide (230 mg, 1.35 mmol) was added. After 30 min, the mixture was partitioned between saturated aqueous NaHCO3 (3 mL) and CHCl3 (5 mL). The aqueous phase was extracted further with CHCl3 (5 mL) and the combined organic layers were dried (Na2SO4), filtered, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography, eluting with hexane:EtOAc—75:25, to give the title compound. MS: m/z=458 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071770B2
Source datasetuspto-grants-2011_12
ORD IDord-097aaaba56cd4b429aef364a2a528f5f
Source noteuspto-grants-2011_12