HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Bromopropane → HCID 67090312, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Bromopropane | HCID 7840 | — |
| Reactant | N-Ethyl-N-methylaniline | HCID 11956 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67090312 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07919629B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-41903f42d8df420aaec451e9b0513004 |
| Source note | uspto-grants-2011_04 |