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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355239Generated: October 30, 2026

Sodium hydride → HCID 68454724, compound

https://huagongshe.com/reaction/2355239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantIndole-5-carbonitrileHCID 27513—
Reactanttert-butyl N-(4-chloro-2-methylbutan-2-yl)carbamateHCID 57429079—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDimethylformamideHCID 6228—
ProductHCID 68454724HCID 68454724—

Reaction Conditions

Temperature50 °C

Reaction Steps

Under a nitrogen atmosphere 4.07 g (16.9 mmol) 5-cyanoindole are dissolved in 30 ml DMF, and 0.73 g (18.3 mmol) sodium hydride (60% dispersion in mineral oil) are added batchwise while cooling with ice and with stirring. Then the mixture is stirred for 30 minutes at ambient temperature. It is heated to 50° C., 0.41 g (1.1 mmol) tetrabutylammonium iodide are added and over a period of 5 hours a solution of N-tert-butoxycarbonyl-3-chloro-1,1-dimethyl-propylamine is added dropwise. Then the mixture is stirred for 18 hours at ambient temperature. Then the reaction solution is poured onto water and extracted with ethyl acetate. The organic phases are combined, dried on sodium sulphate and freed from the solvent in vacuo. The residue is chromatographed on silica gel (petroleum ether/ethyl acetate=100:0→70:30). The product fractions are combined and freed from the solvent in vacuo. The residue is dissolved in 5 ml of methanol and poured onto 50 ml hot water. The precipitate thus obtained is suction filtered and dried in vacuo and reacted further without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754756B2
Source datasetuspto-grants-2010_07
ORD IDord-d6e6a7ba20394a339155b237c11c1604
Source noteuspto-grants-2010_07