HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclopentylamine → N-tert-Butyl-N-cyclopentylthiourea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclopentylamine | HCID 2906 | — |
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-tert-Butyl-N-cyclopentylthiourea | HCID 23003023 | 47% |
Reaction Steps
To a solution of t-butyl isothiocyanate (5.0 mL; 39.41 mmol) in CH2Cl2 (200 mL) was added cyclopentylamine (4.67 mL; 47.29 mmol) followed by DIEA and the reaction mixture was stirred at RT for 2 h. The mixture was diluted with EtOAc, washed with 10% citric acid (2×), saturated NaHCO3 (2×), H2O (2×) and brine (1×). The organic layer was dried over anhydrous MgSO4, filtered and evaporated to dryness to obtain the t-butyl-cyclopentylthiourea as a white solid (3.70 g; 47% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06608027B1 |
| Source dataset | uspto-grants-2003_08 |
| ORD ID | ord-7f25de4ef1be423dbadde0c400952322 |
| Source note | uspto-grants-2003_08 |