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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225599Generated: October 29, 2026

Triphenylarsine → 5-(3,6-Dihydro-2H-pyran-4-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/225599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylarsineHCID 11773—
Reactant2,6-Di-tert-butyl-4-methylphenolHCID 31404—
ReactantLithium ChlorideHCID 433294—
Reactant4-Tributylstannyl-3,6-dihydro-2H-pyranHCID 22252258—
Reactanttert-Butyl 5-iodoisoindoline-2-carboxylateHCID 57753580—
CatalystHCID 178418476HCID 178418476—
SolventDimethylformamideHCID 6228—
Product5-(3,6-Dihydro-2H-pyran-4-yl)-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl esterHCID 5775327074%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution 6.32 mmol 5-iodo-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester (Example A38(b)) in 20 ml DMF were added 12.6 mmol tributyl-(3,6-dihydro-2H-pyran-4-yl)-stannane, 3.79 mmol triphenylarsine, 0.76 mmol bis(triphenylphosphine)palladium(II) chloride, 50.5 mmol lithium chloride and 0.63 mmol 2,6-di-t-butyl-p-cresol and the mixture was heated at 100° C. for 6 h. The reaction mixture was then cooled to room temperature and concentrated in vacuo. The residue was purified by chromatography (SiO2, heptane/ethyl acetate) to yield the title compound as a yellow solid (74% yield). MS (m/e): 246.1 ([M+H−Me2C═CH2]+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557114B2
Source datasetuspto-grants-2009_07
ORD IDord-a8d83dfb2c144a719c7e24eb034e33fb
Source noteuspto-grants-2009_07