HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 15284073, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 15284072 | HCID 15284072 | — |
| Product | HCID 15284073 | HCID 15284073 | — |
Reaction Steps
First, 600 mg of 1,4-bis(6-diethylaminohexyl)-2-nitrobenzene was dissolved in 7 ml of absolute ethanol, and after adding 2.18 g of ethyl iodide at a room temperature with stirring, the mixture was refluxed for 3 hours and then cooled. The reaction mixture was evaporated under a reduced pressure, diluted with 3 ml of acetone, and after adding 1 ml of ethyl acetate allowed to stand in a freezer overnight. Resulting crystal was collected by filtration, washed with acetone/ethyl acetate (1:1), and dried under a reduced pressure to obtain 555 mg of the title compound as a pale yellow crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05093370 |
| Source dataset | uspto-grants-1992_03 |
| ORD ID | ord-be50f7ee1dd2469fafda8c01807627b0 |
| Source note | uspto-grants-1992_03 |