HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminophenol → HCID 20428193, 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 | — |
| Product | HCID 20428193 | HCID 20428193 | — |
Reaction Steps
The process described in Example I was repeated substituting 59.95 parts of m-aminophenol for the p-aminothiophenol and 78.9 parts of bis-(chloropropyl)tetramethyldisiloxane for the bis-(chlorobutyl)tetramethyldisiloxane. The end product was recovered by distillation within the temperature range of from 245° C. to 260° C. under a pressure of from 0.5 mm to 2.0 mm of mercury. This product was identified as bis-(aminophenoxypropyl)tetramethyldisiloxane, a pale yellow liquid which did not solidify upon standing at 0° C. for three days. Its pority, as determined by titration with perchloric acid, exceeded 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04499149 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-0436fba1d5a64e789f34e79e3984a803 |
| Source note | uspto-grants-1985_02 |