HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonia → {[(2R)-oxolan-2-yl]methyl}thiourea
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonia | HCID 222 | — |
| Edukt | Hydrogen Peroxide | HCID 784 | — |
| Edukt | Methanol | HCID 887 | — |
| Edukt | Carbon Disulfide | HCID 6348 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (R)-(-)-Tetrahydrofurfurylamine | HCID 2734124 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | {[(2R)-oxolan-2-yl]methyl}thiourea | HCID 1810731 | — |
Reaktionsschritte
To a 0° C. solution of (R)-(tetrahydrofuran-2-yl)methanamine (5.0 g, 49.5 mmol) and triethylamine (690 uL, 4.95 mmol) in tetrahydrofuran (100 mL) was added carbon disulfide (5.65 g, 74.3 mmol). Stirring was continued for 0.5 hour followed by the dropwise addition of 30% hydrogen peroxide (5.6 g, 49.5 mmol) so that the temperature was maintained below 40° C. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic extract was dried (Na2SO4), filtered and concentrated to afford an oil. The residue was dissolved in tetrahydrofuran, and treated with 7 N ammonia in methanol (14.3 mL, 100 mmol). The precipitate was collected by filtration and washed with water to afford the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08841334B2 |
| Quelldatensatz | uspto-grants-2014_09 |
| ORD ID | ord-ab61ef12de984805b7afab8d21846160 |
| Quellennotiz | uspto-grants-2014_09 |