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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946487Generated: November 2, 2026

Trimethylphosphine → HCID 58460151, compound

https://huagongshe.com/reaction/1946487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylphosphineHCID 68983—
ReactantDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
ReactantTriethyl methanetricarboxylateHCID 80471—
ReactantHCID 58460144HCID 58460144—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58460151HCID 58460151—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of Intermediate 19 (50 mg) and triethylmethanetricarboxylate (0.073 ml) in toluene (1.5 ml) and tetrahydrofuran (1.5 ml), stirred at RT under an inert atmosphere of nitrogen, was added trimethylphosphine, 1M in toluene (0.344 ml). The resulting solution was cooled to −78° C. and diisopropyl azodicarboxylate (0.068 ml) was added dropwise via syringe and the reaction was stirred at −78° C. for 45 mins. The reaction mixture was removed from the cold bath and allowed to warm to RT and stirred under N2 atmosphere overnight. Reaction mixture concentrated in vacuo. The residue was taken up in DCM (20 ml) and washed with water (20 mL). The 2 phases were separated, the organic extract was dried (hydrophobic frit) and concentrated under vacuum. The residue was purified on silica using a cyclohexane:ethyl acetate 0-100% gradient. The desired fractions were combined and concentrated under vacuum to give the title compound (48 mg). LC/MS MH+ 505, Rt 3.41 min (5 minute run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399444B2
Source datasetuspto-grants-2013_03
ORD IDord-7464e1f0a6574e129e7f67c37dccbba0
Source noteuspto-grants-2013_03