Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Solvent | P-Xylene | HCID 7809 | — |
| Product | Benzoic Acid | HCID 243 | — |
Reaction Steps
In a reaction vessel having a capacity of 20 l, 1100 g of the so-obtained block copolymer-containing composition was dissolved in 11 l of p-xylene in a nitrogen atmosphere at 100° C. After the composition had been completely dissolved in p-xylene, 400 ml of pyridine was added into the reaction vessel, and 800 g of benzoyl chloride was continuously supplied in the reaction system over a period of 1 hour. Then, reaction was conducted at 100° C. for 1.5 hours after completion of the addition of benzoyl chloride, and the reaction was stopped by adding 2 l of distilled water into the reaction mixture. After termination of the reaction, the temperature was lowered close to room temperature and the liquid reaction mixture was thrown into a great excess of methanol (in a mixer) to precipitate a benzoic acid-esterified polymer composition. The precipitate was recovered by filtration. After filtration, the benzoic acid-esterified polymer composition was washed with methanol repeatedly and dried under reduced pressure at 50° C. for 24 hours to obtain an intended benzoic acid-esterified polymer composition.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04880873 |
|---|
| Source dataset | uspto-grants-1989_11 |
|---|
| ORD ID | ord-5aac88b3437f48159845792cccfaee68 |
|---|
| Source note | uspto-grants-1989_11 |
|---|