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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Di-tert-butyl diethylphosphoramidite | HCID 4251849 | — |
| Reactant | HCID 42605467 | HCID 42605467 | — |
| Reactant | HCID 178418441 | HCID 178418441 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67279775 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158810B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-b99ddaf3e7904dffa2f9213c72adcd25 |
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| Source note | uspto-grants-2012_04 |
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