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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075293Generated: October 30, 2026

1-Bromopropane → HCID 67090312, compound

https://huagongshe.com/reaction/2075293

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromopropaneHCID 7840—
ReactantN-Ethyl-N-methylanilineHCID 11956—
SolventAcetonitrileHCID 6342—
ProductHCID 67090312HCID 67090312—

Reaction Steps

100 mmol of N-methyl-N-ethylaniline (Aldrich) were quaternized with 100 mmol of bromopropane (Aldrich) at reflux in 100 ml of acetonitrile for 48 hours. After evaporation of the solvent, the N-propyl-N-methyl-N-ethylanilinium bromide (PMEA.Br) obtained was purified by washing with ether. 50 mmol of KBFST were added to 50 mmol of PMEA.Br in 100 ml of water, and then the solution was extracted with twice 50 ml of dichloromethane. After evaporation of the solvent and drying under vacuum, PMEA.BFST was obtained. The two optical isomer forms of this salt were separated on a chiral column. The two optical isomers isolated serve as a chiral reaction medium.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919629B2
Source datasetuspto-grants-2011_04
ORD IDord-41903f42d8df420aaec451e9b0513004
Source noteuspto-grants-2011_04