HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroethanol → HCID 53673190, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | Benzene | HCID 241 | — |
| Reactant | Methacrylic Acid | HCID 4093 | — |
| Reactant | 4-Hydroxy-4'-methoxybiphenyl | HCID 11030839 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | HCID 53673190 | HCID 53673190 | — |
Reaction Steps
4-(methacryloyloxy) ethoxy-4'-methoxybiphenyl is prepared from 4-methoxy-4'hydroxybiphenyl by reaction with ethylenechlorohydrine in aqueous-alcoholic potassium hydroxide solution and subsequent azeotropic esterification with methacrylic acid in chloroform, catalyzed by p-toluol-sulfonic acid. This substance is heated for 8 hours to 65° C. in a benzene solution under nitrogen in the presence of 1 mol percent 2.2-azoisobutylonitrile. The reaction product is dissolved in chloroform and precipitated in a mixture of acetone and methanol. A solution of the liquid-crystal polymer in N-methyl-pyrrolidone is applied via a rubber roller to a glass substrate provided with a conductor structure and dried at 100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04469408 |
| Source dataset | uspto-grants-1984_09 |
| ORD ID | ord-1275b903656e41f6814dbde4c5f8e9bd |
| Source note | uspto-grants-1984_09 |