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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088407Generated: November 2, 2026

Triphenylphosphine → HCID 86653947, compound

https://huagongshe.com/reaction/2088407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPotassium AcetateHCID 517044—
Reactanttert-butyl N-(prop-2-en-1-yl)carbamateHCID 4067274—
Reactant(3-(5-Bromopyrimidin-2-yl)phenyl)methanolHCID 59484879—
CatalystTetrabutylammonium ChlorideHCID 70681—
SolventDimethylformamideHCID 6228—
ProductHCID 86653947HCID 86653947—

Reaction Conditions

Temperature80 °C

Reaction Steps

812 mg (3.06 mmol) of [3-(5-bromopyrimidin-2-yl)phenyl]methanol and 722 mg (4.59 mmol) of tert-butyl N-allylcarbamate are suspended in 16 ml of DMF, and 160 mg (0.61 mmol) of triphenylphosphine, 1.8 g (4.6 mmol) of potassium acetate and 1.28 g (4.59 mmol) of tetra-n-butylammonium chloride are added. The reaction mixture is degassed and flushed with argon, and 137 mg (0.0.61 mmol) of palladium(II) acetate are added under an argon atmosphere. The mixture is heated at 80° C. for 2 h. After cooling, the mixture is filtered off through kieselguhr with suction, and the filtrate is added to water and extracted with 2×100 ml of ethyl acetate, dried over sodium sulfate and evaporated. The product was reacted further without further purification. Yield: 380 mg; HPLC: Rt.=2.66 min (method A); LC-MS: 342 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435986B2
Source datasetuspto-grants-2013_05
ORD IDord-6dfc445f7f104cef96233cf8cb95dda8
Source noteuspto-grants-2013_05