Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfite | HCID 1099 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Disodium disulfite | HCID 24346 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | HCID 131729037 | HCID 131729037 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 87353620 | HCID 87353620 | — |
Reaction Steps
574 g (1.45 mol) di-(2-propylheptyl)-maleate (produced in accordance with Example 2), 40 g of a solution of (a) 70% di-(2-propylheptyl)-sulfosuccinate, (b) 20% water and (c) 10% ethanol (note—the solution of the three components (a), (b) and (c) is obtained as the product of the described synthesis of Example 3. When Example 3 was carried out for the first time, the mixture of components (a), (b) and (c) was not yet available—40.0 g Hydropalat 875 were used instead), 142 g (0.75 mol) sodium disulfite and 194 g deionized water were introduced into a 1-liter four-necked flask equipped with a mechanical stirrer, heating system, reflux condenser and nitrogen inlet and were heated under reflux at 104° C. in a gentle stream of nitrogen until a clear solution was obtained (ca. 3 hours). After stirring for 10 minutes, no more sulfite could be detected in the product. On cooling, the product gelled/solidified which could be avoided by addition of a co-solvent: to this end, 50 g ethanol was added at ca. 80° C. The product thus obtained had the following characteristic data: acid value 0.18 mg KOH/g; Epton: 14.01%; dry residue: 71.66%; sodium sulfate content 0.32%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07981932B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-9aabff25b1744370bb39c6100b82885d |
|---|
| Source note | uspto-grants-2011_07 |
|---|