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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541732Generated: October 31, 2026

Diisopropylethylamine → tert-Butyl {3-[(3-aminophenyl)ethynyl]phenyl}carbamate

https://huagongshe.com/reaction/541732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzenamine, 3-ethynyl-HCID 104682—
Reactanttert-Butyl (3-iodophenyl)carbamateHCID 12990980—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl {3-[(3-aminophenyl)ethynyl]phenyl}carbamateHCID 5796197549%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 3-ethynylaniline (1.16 g, 9.87 mmol) and tert-butyl (3-iodophenyl)carbamate (3.0 g, 9.4 mmol) in THF (28 mL) was treated with bis(triphenylphosphine)palladium(II) chloride (330 mg, 0.47 mmol), copper(I) iodide (140 mg, 0.75 mmol) and N,N-diisopropylethylamine (3.27 ml, 18.8 mmol), and stirred at 25° C. overnight. The reaction was diluted with water and extracted with ethyl acetate three times. The combined organic solutions were dried with sodium sulfate, filtered, and concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (1.42 g, 49%). LCMS for C19H21N2O2 (M+H)+: m/z=309.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-50640c9103914e10afc7c4d77d7d38b8
Source noteuspto-grants-2014_10