Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900486Generated: October 29, 2026

Water → HCID 60147146, compound

https://huagongshe.com/reaction/900486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 60147144HCID 60147144—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTetrahydrofuranHCID 8028—
Solventtetrahydrofuran N,N-dimethylformamideHCID 21974620—
ProductHCID 60147146HCID 6014714689.4%

Reaction Steps

A solution of 5-{2-[4′-(2-benzylbenzofuran-3-yl)-biphen-4-yl]-2-oxoethyl}-2,2-dimethyl-[1,3]dioxane-4,6-dione (200 mg, 0.37 mmol) in THF/DMF (5:1; 6 mL) was added dropwise to a stirred suspension of sodium hydride (95%, 10.2 mg, 0.40 mmol) in anhyd THF (5 mL) at room temperature. The clear solution was stirred at room temperature for 30 min and then a solution of benzyl bromide (76 mg, 0.44 mmol) in THF (5 mL) was added dropwise, followed by the addition of tetra-n-butylammonium iodide (5 mg) as a solid. The reaction mixture was warmed to 60° C. for 4 h (TLC control), cooled to room temperature and then water (10 mL) was added cautiously. The reaction mixture was extracted with diethyl ether (3×15 mL). The combined organic extracts were washed successively with water (2×10 mL), sat'd aq NaCl (3×10 mL), dried over anhyd MgSO4, filtered and concentrated in vacuo. Purification by trituration and filtration from MeOH afforded the title compound as a pale yellow solid (210 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358364B2
Source datasetuspto-grants-2008_04
ORD IDord-89e9f93b498b4eab9a10c8a0045aa424
Source noteuspto-grants-2008_04