HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 54190602, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 18920666 | HCID 18920666 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 54190602 | HCID 54190602 | — |
Reaction Steps
1 ,2-di(p-bromophenyl)-hydroxyethane (17.8 g, 0.05 mol), potassium iodide (165 g), copper (I) iodide (95 g) and hexamethylphosphoramide (200 mL) was stirred at 150-160° C. for 48 h and then cooled. Work-up was as described in Example IV to provide a light yellow solid (10 g), which was the expected 1,2-di(p-iodophenyl)-1-hydroxyethane. A portion of this compound (7.2 g, 0.016 mol), acetic anhydride (16 mL), pyridine (16 mL) were heated at 60° C. for 30 min, followed by standing for 2 days. The resulting solution was worked up as in Example IlIl to provide an oil which solidified upon standing. The solid was crystallized from hexanes to provide the title compound as a light yellow solid (4.3 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753757 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-4f3a1ab3940b40c2b87ff8c166261605 |
| Source note | uspto-grants-1998_05 |