HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 129653Generated: October 27, 2026
Acetic Acid → (4-Octyloxyphenyl)phenyliodonium tosylate
https://huagongshe.com/reaction/129653
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Octyl phenyl ether | HCID 74558 | — |
| Reactant | Hydroxy tosyloxy iodobenzene | HCID 21918218 | — |
| Solvent | Water | HCID 962 | — |
| Product | (4-Octyloxyphenyl)phenyliodonium tosylate | HCID 22131423 | — |
Reaction Steps
22.2 g (or 0.057 mol) of hydroxy-tosyloxyiodobenzene, 9 g (or 0.04 mol) of n-octyl phenyl ether, 5 ml of acetonitrile and 1.5 ml of acetic acid were charged into a 250 ml Erlenmeyer flask equipped with a magnetic stirrer bar. This mixture was stirred and was heated to a temperature of 40° C. for 2 hours, 30 minutes. 1.5 ml of glacial acetic acid was then added and the mixture was then maintained for 5 hours at 40° C. The reaction mixture was permitted to cool and 150 ml of water were added while stirring vigorously. This mixture was then stirred for 12 hours at room temperature and was then separated. The organic phase was washed several times with water, until a yellow precipitate appeared. This solid was recovered by filtration, was washed with 50 ml of ether and was then dried under vacuum at a temperature of 45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05468902 |
|---|
| Source dataset | uspto-grants-1995_11 |
|---|
| ORD ID | ord-10c8a5c162f843e7a8058afe2b6f543d |
|---|
| Source note | uspto-grants-1995_11 |
|---|