HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2,4-Difluorophenyl)thiocarbamic acid O-(6-hydroxymethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ylmethyl)ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Difluoro-1-isothiocyanatobenzene | HCID 518879 | — |
| Reactant | 6,6-Bis(hydroxymethyl)-6,7,8,9-tetrahydrobenzocyclohepten-5-one | HCID 67073086 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2,4-Difluorophenyl)thiocarbamic acid O-(6-hydroxymethyl-5-oxo-6,7,8,9-tetrahydro-5H-benzocyclohepten-6-ylmethyl)ester | HCID 11964900 | — |
Reaction Steps
To a solution of 6,6-bis(hydroxymethyl)-6,7,8,9-tetrahydrobenzocyclohepten-5-one (500 mg, 2.27 mmol) in 28 ml of tetrahydrofuran were added, at room temperature, triethylamine (0.35 ml, 2.50 mmol) and 2,4-difluorophenyl isothiocyanate (740 μl, 5.68 mmol). The mixture was heated to reflux for 72 hours, concentrated and purified by column chromatography on silica gel (eluent: 1:2 tert-butyl methyl ether/cyclohexane). The product was obtained in a yield of 234 mg (26%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858613B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-c87134869d694f10a3d7af0207b56e2a |
| Source note | uspto-grants-2010_12 |