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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2190932Generated: October 30, 2026

Benzyl Bromide → HCID 67523754, compound

https://huagongshe.com/reaction/2190932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant4H-1,3-Benzodioxin-4-one, 5-hydroxy-2,2-dimethyl-HCID 11052514—
SolventDimethylformamideHCID 6228—
ProductHCID 67523754HCID 6752375484.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a mixture of 5-hydroxy-2,2-dimethyl-benzo[1,3]dioxin-4-one (Uchiyama M. et al Org. Lett. 2006, 8(24), 5517-5520) (2.0 g, 10.4 mmol) and benzyl bromide (1.78 g, 10.4 mmol) in DMF in an ice bath was added sodium hydride (60% dispersed in mineral oil, 624 mg, 15.6 mmol). Resulting mixture was stirred at 0° C. for 10 min and then at rt for 6 h. Reaction mixture was quenched with water (250 mL), neutralized using 1 N HCl to pH=6-7 and extracted with EtOAc (2×). Combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated. Crude product was triturated with hexanes (50 mL). Solid was collected and dried in vacuo to provide the title compound 2.5 g. 1H NMR (200 MHz, CDCl3): δ (ppm)=7.54 (m, 2H), 7.37 (m, 4H), 6.57 (m, 2H), 5.25 (s, 2H), 1.71 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324405B2
Source datasetuspto-grants-2012_12
ORD IDord-6a6437b19baa452380e8dcc2f1b034b3
Source noteuspto-grants-2012_12