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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983926Generated: October 26, 2026

Water → Pent-4-en-1-yl-7-vinyl-1H-indole

https://huagongshe.com/reaction/983926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-Pentene, 5-bromo-HCID 70704—
Reactant7-Ethenyl-1H-indoleHCID 14567404—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductPent-4-en-1-yl-7-vinyl-1H-indoleHCID 2255682173.1%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a 0° C. solution of 7-vinylindole (5.0 g, 34.9 mmol) in 140 mL of dimethylformamide was added sodium hydride (60% dispersion in mineral oil) (3.5 g, 87.3 mmol). The ice bath was removed and the solution was warmed to 20-24° C. and stirred an additional 30 minutes. 5-Bromo-1-pentene (20 mL, 175 mmol) was added dropwise and stirring continued for 3 hrs. The solution was poured into 150 mL of water and 150 mL of ethyl acetate. The aqueous layer was washed with additional ethyl acetate (3×100 mL) and the combined organic layers were washed with saturated aqueous sodium chloride, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 5-10% ethyl acetate in hexanes. Fractions containing product were combined and concentrated under reduced pressure to provide 5.39 g (73%) of the desired compound as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867198B2
Source datasetuspto-grants-2005_03
ORD IDord-0b752ee2e1214e71ab30f2e14ee6d829
Source noteuspto-grants-2005_03