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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983928Generated: October 30, 2026

Allyl bromide → HCID 22556853, compound

https://huagongshe.com/reaction/983928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22556802HCID 22556802—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 22556853HCID 2255685391%

Reaction Conditions

Temperature22 °C

Reaction Steps

To a 0° C. solution of N-[tert-butoxycarbonyl] N-allyl N-[(1H-indol-7-yl)methyl]amine (6.6 g, 23 mmol) in anhydrous dimethylformamide was added slowly sodium hydride (60% dispersion in mineral oil, 1.75 g, 43.7 mmol). The mixture was warmed to 20-24° C. and stirred for 30 minutes, followed by the addition of allyl bromide (4.0 mL, 46 mmol). The reaction was then stirred at 20-24° C. overnight. The reaction mixture was diluted with ethyl acetate (450 mL), washed with water (2×100 mL), saturated aqueous sodium chloride (150 mL), and the organic layer dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was subjected to silica gel chromatography, eluting with 10% ethyl acetate in hexanes. Fractions containing product were combined and concentrated under reduced pressure to provide 6.8 g (91%) of the desired compound as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867198B2
Source datasetuspto-grants-2005_03
ORD IDord-c37238b360c746a4a8292c3bc508a8c7
Source noteuspto-grants-2005_03