Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Styrene | HCID 7501 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | N-(hydroxymethyl)phthalimide | HCID 8354 | — |
| Reactant | 1,2-Diethenylbenzene | HCID 66666 | — |
| Product | Hydrochloric Acid | HCID 313 | — |
| Product | L-Valine | HCID 6287 | — |
Reaction Steps
700 g of N-hydroxymethyl phthalimide, dissolved in 2400 g of dichlorethane, are heated for 5 hours to reflux temperatures with 454 g of acetic acid anhydride. 300 g of a styrene polymer crosslinked with 6 % of divinyl benzene are swollen in this ester solution over a period of 30 minutes at 60° C. 400 g of concentrated sulphuric acid are then added dropwise over a period of 4 hours at reflux temperature. After stirring for 20 hours at the same temperature, the polymer is filtered off under suction and suspended in 2000 ml of 10 % aqueous ammonia solution. The residues of swelling agent are removed from the suspension by azeotropic distillation. The polymer is then heated for 10 hours to 180° C with 40 % sodium hydroxide solution in an autoclave. After the sodium hydroxide has been washed out, 750 ml of a weakly basic anion exchanger are obtained with an acid binding capacity of 3.3 Val/1 for N/10 hydrochloric acid and a nitrogen content of 9.55 % in the dry material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03989650 |
|---|
| Source dataset | uspto-grants-1976_11 |
|---|
| ORD ID | ord-e4825bbebfda48d08a319d57647e4ce6 |
|---|
| Source note | uspto-grants-1976_11 |
|---|