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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280331Generated: October 28, 2026

Allyl bromide → HCID 17896911, compound

https://huagongshe.com/reaction/1280331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
Reactant5,6-Dihydroindeno[2,1-b]indoleHCID 13129410—
CatalystHexadecyltrimethylammonium BromideHCID 5974—
SolventBenzeneHCID 241—
ProductHCID 17896911HCID 1789691137%

Reaction Steps

In a 0.5 l bulb were placed 100 ml 50% aqueous NaOH, 100 ml benzene, 6.1 g (28 mmol)of 5,6-dihydroindeno[2,1-b]indole, prepared in Example 4, 5 g (41 mmol) of allyl-bromide and 0.5 g of trimethylcetylammonium bromide. After having stirred the obtained mixture for 12 hours, the formation of an organic phase was observed; said phase was separated, washed twice with water (100 ml) and dried over Na2SO4. After removal of the solvent, the residue was passed through a column of silicagel, eluted with hexane/ethylacetate=5:1); the resulting solution was evaporated, obtaining 1.8 g of N-allyl-5,6-dihydroindeno[2,1-b]indole (yield=37%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451724B1
Source datasetuspto-grants-2002_09
ORD IDord-ae87bebf6ca440a494c85c3ae9f11f1d
Source noteuspto-grants-2002_09