HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 4-[3-[Ethyl[3-(phenylthio) propyl]amino]-2-hydroxypropoxy]-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloropropyl phenyl sulfide | HCID 269606 | — |
| Reactant | 4-[3-(Ethylamino)-2-hydroxypropoxy]-benzonitrile | HCID 15066841 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-[3-[Ethyl[3-(phenylthio) propyl]amino]-2-hydroxypropoxy]-benzonitrile | HCID 15158813 | — |
Reaction Steps
5.0 g of 4-[3-(ethylamino)-2-hydroxypropoxy]-benzonitrile and 4.0 g of 1-chloro-3-(phenylthio) propane was dissolved in 70 ml of acetonitrile and mixed with 6.4 g potassium carbonate and 8.0 g of sodium iodide. The mixture was refluxed over night, filtrated, evaporated and the residue was dissolved in 2 M hydrochloric acid. This acidic waterlayer was washed with two portions of diethylether, alkalized with 10 M sodium hydroxide and extracted with three portions of dichlorometane. The combined layers of dichloromethane were dried over sodium sulphate and evaporated. The oily residue was purified by column chromatography on silica gel. Yield: 2.1 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034411 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-bf82bb9fe8d34ba0a569d0bd55d8b34a |
| Source note | uspto-grants-1991_07 |