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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388888Generated: November 4, 2026

Dimethylamine → HCID 13055164, compound

https://huagongshe.com/reaction/1388888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantHCID 12834669HCID 12834669—
SolventDichloromethaneHCID 6344—
ProductHCID 13055164HCID 13055164—

Reaction Steps

The starting material is prepared as follows: 3.8 g of 3-chloro-6-o-tolyl-benzonitrile (described in Example 3) is brominated as described in Example 2, and the residue dissolved in 25 ml of methylene chloride. The solution is added slowly to that of 14 g of liquid dimethylamine in 100 ml of methylene chloride while stirring at 0°. The mixture is stirred at room temperature for 16 hours, evaporated and the residue stirred with diethyl ether and 1 N hydrochloric acid. The aqueous phase is separated, combined with methylene chloride and basified with cold 2 N aqueous sodium hydroxide. The organic layer is separated, dried and evaporated to yield the 3-chloro-6-(o-dimethylaminomethyl-phenyl)-benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04434100
Source datasetuspto-grants-1984_02
ORD IDord-1c58959e882242a0b52cd52d2a225543
Source noteuspto-grants-1984_02