HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminophenol → HCID 20428218, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | 4-Aminothiophenol | HCID 14510 | — |
| Reactant | HCID 20428219 | HCID 20428219 | — |
| Reactant | HCID 20836576 | HCID 20836576 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 20428218 | HCID 20428218 | — |
Reaction Steps
The process of Example XIX was again practiced except that 59.95 parts of m-aminophenol was substituted for the p-aminothiophenol and 78.9 parts of Bis-(chloropropyl)tetramethyldisiloxane was substituted for the Bis-(chlorobutyl)tetramethyldisiloxane, and the phase transfer catalyst was 3 grams of 18 crown -6 ether. The end product was recovered at a temperature within the range of from 245° C. to 260° C. at from 0.5 mm to 2.0 mm of mercury. The recovered product was identified as Bis-(m-aminophenoxypropyl)tetramethyldisiloxane. The recovered product material was a pale yellow liquid which did not solidify upon standing in the cold at 0° C. for 3 days. Its purity, as determined by titration with perchloric acid, was better than 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04499149 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-593adb76224a44c78b7ebd115de46b70 |
| Source note | uspto-grants-1985_02 |