HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Trifluoromethyl)aniline → 2-(Trifluoromethyl)phenyl isothiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Trifluoromethyl)aniline | HCID 6922 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(Trifluoromethyl)phenyl isothiocyanate | HCID 737162 | — |
Reaction Steps
2-trifluoromethylaniline (4.1 ml, 0.0325 mol) is added dropwise at a temperature close to 20° C. and under an argon atmosphere to a mixture containing thiophosgene (2.5 ml, 0.0326 mol) in 43 ml of water. Agitation is carried out for twelve hours then 30 ml of ethyl acetate is added. The organic phase is extracted with water then with a solution of 10% sodium bicarbonate and finally with a solution of salt water. The organic phase is dried over magnesium sulphate and the solvent is evaporated off with a rotary evaporator. The product obtained (6.85 g, 100%) is in the form of a brown oil which is used immediately for the following reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07015213B1 |
| Source dataset | uspto-grants-2006_03 |
| ORD ID | ord-f07156a3ec2e470abf4e8d3f91fb829b |
| Source note | uspto-grants-2006_03 |