HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 3-Cyano-5-methoxy-2-(trifluoromethyl)indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chlorosulfonyl isocyanate | HCID 70918 | — |
| Reactant | 5-Methoxy-2-(trifluoromethyl)-1H-indole | HCID 15335343 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Cyano-5-methoxy-2-(trifluoromethyl)indole | HCID 15335344 | 25% |
Reaction Steps
A solution of 5-methoxy-2-(trifluoromethyl)indole (3.0 g, 13.0 mmole) in acetonitrile is treated dropwise with chlorosulfonyl isocyanate (2.02 g, 14.3 mmole) at 0° C., stirred at ambient temperatures for 2.5 hours, treated with dimethylformamide (DMF) (2.1 g, 28.6 mmole), stirred at ambient temperatures for 0.75 hour and poured into water. The resultant mixture is extracted with diethyl ether. The combined extracts are washed sequentially with water and brine, dried over MgSO4 and concentrate in vacuo to give a brown oil residue. The oil is crystallized in ether/hexanes to give the title product as brown crystals, 0.78 g (25% yield), mp 189°-190° C., identified by IR, 1HNMR, 13CNMR and 19FNMR.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05599832 |
| Source dataset | uspto-grants-1997_02 |
| ORD ID | ord-7f48494cadb8424aa2e18f8ddf2adcc3 |
| Source note | uspto-grants-1997_02 |