Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | Anisole | HCID 7519 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18759331 | HCID 18759331 | — |
Reaction Steps
There was added dropwise, 45.6 grams (0.24 mole) of 40% peracetic acid to 20.4 grams (0.1 mole) of iodobenzene while the temperature was maintained at less than 30° C. After the addition of the peracid, there was added to the resulting mixture 19.05 grams (0.1 mole) of p-toluene sulfonic acid monohydrate, 10.8 grams (0.1 mole) of anisole and 10 ml of glacial acetic acid. The resulting mixture was stirred for 2 hours. The 4-methoxyphenyliodonium tosylate was isolated from the reaction mixture by trituration with diethyl ether, filtering and further washing with diethyl ether. There was obtained 41.8 grams or an 86.7% yield of a product having a melting point of 163°-165° C. Based on method of preparation, the product was 4-methoxyphenyliodonium tosylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04399071 |
|---|
| Source dataset | uspto-grants-1983_08 |
|---|
| ORD ID | ord-84a2bce1a08b4e70991b1c71795b7af3 |
|---|
| Source note | uspto-grants-1983_08 |
|---|