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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1411318Generated: November 2, 2026

Tributylstannane → tert-Butyl 5-(trifluoromethyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylate

https://huagongshe.com/reaction/1411318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylstannaneHCID 5948—
ReactantAzobisisobutyronitrileHCID 6547—
Reactanttert-butyl 3-(((2-bromo-4-(trifluoromethyl)phenyl)amino)methyl)-2,5-dihydro-1H-pyrrole-1-carboxylateHCID 90449914—
SolventBenzeneHCID 241—
Producttert-Butyl 5-(trifluoromethyl)spiro[indoline-3,3'-pyrrolidine]-1'-carboxylateHCID 9044964742.2%

Reaction Steps

tert-Butyl 3-(((2-bromo-4-(trifluoromethyl)phenyl)amino)methyl)-2,5-dihydro-1H-pyrrole-1-carboxylate (6.46 g, 15.3 mmol) was dissolved in benzene (300 mL). Thereafter, tributyltin hydride (6.02 mL, 23.0 mmol) and azobisisobutyronitrile (380 mg, 2.31 mmol) were added to the above obtained solution at room temperature, and the thus obtained mixture was then stirred for 15 hours while heating under reflux. Thereafter, the reaction solution was concentrated in vacuo, and the obtained residue was then purified by silica gel column chromatography (hexane:ethyl acetate=3:1) to obtain tert-butyl 5-(trifluoromethyl)spiro[indoline-3,3′-pyrrolidine]-1′-carboxylate (2.21 g, 42%) in the form of a colorless amorphous product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921576B2
Source datasetuspto-grants-2014_12
ORD IDord-f9ad2439c7b84deb84947f4d54b3e6d9
Source noteuspto-grants-2014_12