HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 10435-44-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Reactant | 10435-44-6 | HCID 3014639 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 10435-44-6 | HCID 3014639 | 83.7% |
| Product | HCID 4094028 | HCID 4094028 | — |
Reaction Steps
A series of di-n-butyl ammonium salts were prepared utilizing an absolute ethanol solution of di-N-butylamine. In preparing di-n-butylammonium bromide, hydrogen bromide gas was introduced into a solution of 585 grams of di-n-butylamine in absolute ethanol until the solution was saturated. The reaction vessel was in an ice bath during the addition. The solution was then treated with ether followed by further cooling to induce crystallization. The product was isolated by filtration, washed thoroughly with ether, and dried for about 12 hours in a vacuum oven (80° C. at about 15 torr). There was obtained an 83.7% yield of di-n-butylammonium bromide, MP 295°-296.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04863984 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-94ccafa9279747bd8d2713525ab79362 |
| Source note | uspto-grants-1989_09 |