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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766922Generated: October 31, 2026

Water → HCID 46834506, compound

https://huagongshe.com/reaction/1766922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 46834505HCID 46834505—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 46834506HCID 4683450659%

Reaction Steps

To a solution of diallyl [8-[(tert-butyldimethylsilyl)oxymethyl]-1-naphthyl]methyl phosphate (5.01 g, 10.8 mmol) obtained from Example 25-(1) in tetrahydrofuran (50 ml) was added tetrabutylammonium fluoride (1 mol/l tetrahydrofuran solution; 13.5 ml, 13.5 mmol), and the mixture was stirred at room temperature for 1 hour. Water was added and the product was extracted with ethyl acetate. The organic layer was concentrated under reduced pressure to give an oily residue. The residue was subjected to chromatography on a silica gel (75 g) column (eluent; ethyl acetate:hexane=3:1˜4:1) to afford the title compound (2.22 g, 59% yield) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230023B2
Source datasetuspto-grants-2007_06
ORD IDord-230eff1f3d3e4f808fc625a458dbdcc8
Source noteuspto-grants-2007_06