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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 376898Generated: October 30, 2026

Hydrochloric Acid → HCID 11951932, compound

https://huagongshe.com/reaction/376898

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethylamineHCID 6329—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
Reactant2-Chloro-5-(trifluoromethyl)benzaldehydeHCID 688181—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11951932HCID 11951932—

Reaction Steps

2.1 g of 2-chloro-5-trifluoromethylbenzaldehyde, 15 ml of methylamine and 2 g of magnesium sulfate were stirred at room temperature for 2 h, the excess methylamine for the most part evaporating. The reaction mixture was diluted with ether, filtered and concentrated in vacuo. The methylbenzimine thus obtained was dissolved in 15 ml of THF and added dropwise to a suspension of 1.5 g of sodium borohydride in 15 ml of THF. After stirring overnight, the mixture was treated with 30 ml of methanol, stirred for a further 30 min and then rendered acidic with dil. hydrochloric acid. It was extracted with tert-butyl methyl ether, and the aqueous phase was rendered alkaline and extracted twice again with tert-butyl methyl ether. After concentrating this extract, 1.0 g of N-(2-chloro-5-trifluoromethylbenzyl)-N-methylamine was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06022899
Source datasetuspto-grants-2000_02
ORD IDord-14f7924a83e74a80bd6f1ef440149a7d
Source noteuspto-grants-2000_02