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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694666Generated: November 1, 2026

Di-tert-butyl diethylphosphoramidite → HCID 67279775, compound

https://huagongshe.com/reaction/1694666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butyl diethylphosphoramiditeHCID 4251849—
ReactantHCID 42605467HCID 42605467—
ReactantHCID 178418441HCID 178418441—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67279775HCID 67279775—

Reaction Steps

To a solution of 7-({2-[5-fluoro-3-(trifluoromethyl)phenyl](1,3-oxazol-4-yl)}methoxy)-3-(4-hydroxyphenyl)chromen-4-one (1 g, 2.01 mmol) in tetrahydrofuran (50 mL) was added 1-H-tetrazole (3% wt in acetonitrile, 65 ml, 22.1 mmol), followed by di-tert-butyl N,N-diethylphosphoramidite (2.57 ml, 4.6 mmol). After stirring at room temperature for 2 hours, the reaction mixture was diluted with methylene chloride and washed with saturated sodium bicarbonate. The organic layer was separated, and the aqueous layer extracted twice more with methylene chloride. The combined extracts were dried over sodium sulfate, and solvent removed under reduced pressure. The residue was purified by biotage column chromatography, eluting with ethyl acetate/hexane mixture (1:4) to afford 3-{4-[bis(tert-butoxy)phosphinooxy]phenyl}-7-({2-[5-fluoro-3-(trifluoromethyl)phenyl](1,3-oxazol-4-yl)}methoxy)chromen-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158810B2
Source datasetuspto-grants-2012_04
ORD IDord-b99ddaf3e7904dffa2f9213c72adcd25
Source noteuspto-grants-2012_04