HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → HCID 86596158, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | HCID 23019728 | HCID 23019728 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86596158 | HCID 86596158 | 38.4% |
Reaction Steps
84 mg (0.36 mmol) of 4-(2′-cyanoisoindolyl)aniline was suspended in 40 mL of a mixture of benzene and tetrahydrofuran (1:1, v/v) and refluxed for 1 hour in the presence of 65 mg (0.64 mmol) of triethylamine and 40 mg (0.35 mmol) of thiophosgene. The reaction mixture was concentrated under a vacuum, and then the residue was recrystallized with acetonitrile to obtain 37 mg of the titled 4-(2′-cyanoisoindolyl)phenylisothiocyanate expressed by the following formula in the form of a colorless needle crystal.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08183060B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-53cd11d598454faaa9eee88e90bf0b4e |
| Source note | uspto-grants-2012_05 |