HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 3,4-Dimethoxyphenyldisulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Acetic acid, 2-fluoro-, 1,1'-anhydride | HCID 67886 | — |
| Reactant | 3,4-Dimethoxybenzenesulfonyl chloride | HCID 2734183 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3,4-Dimethoxyphenyldisulfide | HCID 11267746 | — |
Reaction Steps
3,4-dimethoxyphenylsulfonyl chloride (2.3 mmol) was dissolved in acetone (60 mL), and then NaI (3.4 g, 23 mmol) and fluoroacetic anhydride (1.45 mL, 6.9 mmol) were added and the mixture was stirred at room temperature for one hour. The reaction solution was concentrated, water was added, extraction was performed with ether and the organic layer was further washed with aqueous sodium thiosulfate, water and saturated saline. After drying over magnesium sulfate and vacuum concentration, the residue was purified with a silica gel column (hexane) to obtain 3,4-dimethoxyphenyldisulfide as a light yellow crystalline compound (58% yield). The NMR and mass spectral data for the obtained compound were as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06900307B1 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-03b07f8954b243fda6cc6cb8b2bc2cb9 |
| Source note | uspto-grants-2005_05 |