HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethylcarbamoyl chloride → 1,1-Diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethylcarbamoyl chloride | HCID 6916 | — |
| Reactant | 6,7,8,9-Tetrahydro-dibenzofuran-2-ylamine | HCID 2794782 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1,1-Diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea | HCID 24898075 | 54.5% |
Reaction Steps
Diethylcarbamoyl chloride (0.72 mL, 5.5 mmol) was added to a solution of 6,7,8,9-tetrahydro-dibenzofuran-2-ylamine (0.94 g, 5.0 mmol) in pyridine (15 mL). The reaction mixture was stirred overnight at room temperature. The crude material was diluted in chloroform and washed with 1 N HCl, water, and brine, dried (Na2SO4) and concentrated. The crude material was recrystallized from acetonitrile to provide 1,1-diethyl-3-(6,7,8,9-tetrahydro-dibenzofuran-2-yl)-urea (0.78 g). Mp 179-180° C.; Anal. Calcd. for C17H22N2O2: C, 71.30; H, 7.74; N, 9.78; Found: C, 71.29; H, 7.66; N, 9.72.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07601856B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-b5f848d6e7b44f8ba556ec37dba7bf2f |
| Source note | uspto-grants-2009_10 |