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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225611Generated: October 29, 2026

Tetramethyltin → 5-Methyl-6-morpholin-4-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl Ester

https://huagongshe.com/reaction/225611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetramethyltinHCID 11661—
ReactantCesium fluorideHCID 25953—
Reactant5-Chloro-6-morpholin-4-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl esterHCID 57753302—
CatalystHCID 178418851HCID 178418851—
Solvent1,4-DioxaneHCID 31275—
Product5-Methyl-6-morpholin-4-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl EsterHCID 5775337743%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution 0.38 mmol 5-chloro-6-morpholin-4-yl-1,3-dihydro-isoindole-2-carboxylic acid tert-butyl ester (Example A44(a)) in 3 ml dioxane were added 0.02 mmol bis(tri-tert-butylphosphine)palladium(0), 0.84 mmol cesium fluoride and 0.77 mmol tetramethylstannane and the mixture was heated at 80° C. for 5 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 light yellow solid (43% yield). MS (m/e): 219.4 ([M+H−Me2C═CH2]+, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557114B2
Source datasetuspto-grants-2009_07
ORD IDord-9325484dd21440a0aa013189ce40eed2
Source noteuspto-grants-2009_07