HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → Bisphenol A
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Bisphenol A | HCID 6623 | — |
| Reactant | N,N-Dimethyl-1,3-propanediamine | HCID 7993 | — |
| Reactant | 1,1-Propanediamine | HCID 14954072 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | Bisphenol A | HCID 6623 | — |
| Product | N,N-Dimethylpropanediamine | HCID 169191 | — |
Reaction Steps
A 0.05 mole sample of bis-phenol A was dissolved in an ethanol-water solution containing 95% ethanol. This solution then was added dropwise to a 0.05 mole fraction of N,N-dimethyl-1,3-propanediamine sample dispersed in 50 milliliters of an ethanol-water solution containing 95% ethanol. The addition of the bis-phenol A fraction to the propanediamine sample was at room temperature (70° F.) over a 15 minute period. There was a slight exotherm during the addition. After all the bis-phenol A was added, the solution was stirred for an hour and then the solvent flashed using a rotary vacuum distillation apparatus. The residual solids were transferred to a vacuum oven to dry, and a N,N-dimethylpropanediamine salt of bis-phenol A was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04250293 |
| Source dataset | uspto-grants-1981_02 |
| ORD ID | ord-658c1f9f59a64f80b56791fc6585e1e4 |
| Source note | uspto-grants-1981_02 |