HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stearyl Alcohol → HCID 19812763, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stearyl Alcohol | HCID 8221 | — |
| Reactant | 2-Fluorotetracene-5,12-dione | HCID 20089828 | — |
| Product | HCID 19812763 | HCID 19812763 | — |
Reaction Steps
The procedure is analogous to Example 1, and 2-fluorotetracene-5,12-dione is reacted with 1-octadecanol, the 2-n-octadecyloxytetracene-5,12-dione obtained is converted into the corresponding diacetate by reductive acetylation, and the latter is reacted with sulfur int eh presence of p-toluenesulfonic acid to form 2-n-octadecyloxytetracene-5,6,11,12-tetrathiotetracene. The individual reaction products have the following characteristic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05158829 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-80277538c25a404db0fc52f5e8a70224 |
| Source note | uspto-grants-1992_10 |