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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796575Generated: November 2, 2026

Potassium phosphide (K3P) → HCID 85865003, compound

https://huagongshe.com/reaction/1796575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium phosphide (K3P)HCID 62745—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantDimesitylphosphineHCID 4590857—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 85865003HCID 85865003—

Reaction Conditions

Temperature-78 °C

Reaction Steps

KHMDS (35 mL of a 0.5 M solution in toluene, 17.5 mmol, Aldrich) 35 was added to a solution of dimesitylphosphine (4.1 g, 15.8 mmol) in THF (50 mL) at −78° C. After stirring for 20 min at −78° C. bromoacetaldehyde diethylacetal (2.85 mL, 19 mmol, Aldrich) was added dropwise to the solution of potassium phosphide. The solution was stirred for 5 min at −78° C., warmed to RT and stirred for 30 min at RT. Assay by 31P-NMR (crude reaction mixture) showed the formation of product (−29.5 ppm). The solvent was evaporated, the residue was flushed through a 6×3.3 cm plug of silica gel and toluene was removed (aspirator) to afford the product as a yellow oil. The product was dissolved in a mixture of degassed acetone (60 mL) and 5% aq. HCl (30 mL) and refluxed under Ar for 2.5 h. A saturated, degassed solution of NaHCO3 (100 mL) was added to the reaction mixture followed by extraction with degassed CH2Cl2 (3×50 mL). The solution was evaporated under Ar followed by filtration through a plug of silica gel (9×3.6 cm; Ar atmosphere), CH2Cl2 eluent, collecting 250 mL. Evaporation afforded product as a very air-sensitive white solid, 4.1 g (83.1%). 31P{1H} NMR (CD2Cl2): −35.6 ppm (s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030200B2
Source datasetuspto-grants-2006_04
ORD IDord-06a57014a49d4ecf92b26b854081f05e
Source noteuspto-grants-2006_04