HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Aminoacetophenone → HCID 54333435, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | HCID 54204630 | HCID 54204630 | — |
| Solvent | Hexamethylphosphoramide | HCID 12679 | — |
| Product | HCID 54333435 | HCID 54333435 | — |
Reaction Steps
p-Aminoacetophenone is heated with 5 g. 10-(2-thien-yl)-1-methanesulfonyloxy-9-decene (prepared by the method of Example 9) in 50 ml. hexamethylphosphoramide containing anhydrous potassium carbonate (1.9 g.) for 16 hours a 100° C. The solution is cooled to room temperature, filtered to remove solids, and the filtrate is diluted with cold water (50 ml.). The amber solid so obtained is collected and washed with water. Recrystallization from ethanol followed by dichloromethane provides the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04211783 |
| Source dataset | uspto-grants-1980_07 |
| ORD ID | ord-1621db1e19aa48b7b115d95afb854ace |
| Source note | uspto-grants-1980_07 |