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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855973Generated: October 31, 2026

Dichloromethane → HCID 23347209, compound

https://huagongshe.com/reaction/1855973

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactant2-(Diisopropylamino)ethyl chlorideHCID 7312—
ReactantSodium HydroxideHCID 14798—
Reactant2-(1-bromonaphthalen-2-yl)acetonitrileHCID 234377—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
ProductHCID 23347209HCID 23347209—

Reaction Steps

69 Parts of α-(1-bromo-2-naphthyl)acetonitrile is stirred in 150 parts by volume of 50% sodium hydroxide and then 0.7 parts of benzyltriethylammonium chloride is added to the mixture. To this mixture is added slowly a solution of 41.82 parts of 2-chloro-N,N-diisopropylethylamine in 150 parts by volume of methylene chloride and the resulting mixture is stirred at room temperature for about 2 hours. Then, additional quantities of methylene chloride and water are added to the reaction mixture. The organic layer is then separated, dried over anhydrous sodium sulfate and concentrated to give α-(1-bromo-2-naphthyl)-α-[2-(diisopropylamino)ethyl]acetonitrile, as a solid. This compound is represented by the following structural formula ##STR34##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04217306
Source datasetuspto-grants-1980_08
ORD IDord-8701bd3674de421b99f7d9784aff6bef
Source noteuspto-grants-1980_08