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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178322Generated: November 1, 2026

Allyl bromide → HCID 23117635, compound

https://huagongshe.com/reaction/1178322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium HydroxideHCID 14798—
ReactantBis(tetrabutylammonium) sulphateHCID 11433187—
ReactantHCID 58696280HCID 58696280—
SolventDichloromethaneHCID 6344—
ProductHCID 23117635HCID 23117635—

Reaction Steps

Ethyl(benzylidene-amino)-(3,4-dichlorophenyl)acetate (425 g) was dissolved in methylene chloride (1.8 L). 10N Aqueous sodium hydroxide (1.2 L), allyl bromide (158 mL), and tetrabutylammonium sulfate (41 g) were added to the resultant solution, followed by stirring at room temperature for one hour. The reaction mixture was subjected to partitioning. Water (1 L) was added to the aqueous layer, and then the mixture was extracted with methylene chloride. The thus-obtained organic layer was washed with saturated brine, dried over sodium sulfate anhydrate, and concentrated under reduced pressure, to thereby give the title compound (518 g). The title compound was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07276511B2
Source datasetuspto-grants-2007_10
ORD IDord-1c53244836ad429c81e46983e8c7443d
Source noteuspto-grants-2007_10