HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hexane → N-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Benzoyl isothiocyanate | HCID 68284 | — |
| Reactant | 2-Amino-2-ethylbutan-1-ol | HCID 14325607 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamide | HCID 86618579 | 80.1% |
Reaction Steps
Benzoyl isothiocyanate (4.28 mL, 31.8 mmol) was added under nitrogen to a solution of 2-amino-2-ethylbutan-1-ol (3.7315 g, 31.8 mmol), prepared in the previous step, in 100 mL of anhydrous tetrahydrofuran (exotherm on addition). After the addition, the reaction was refluxed for 2.5 h. After cooling to room temperature, 100 mL of hexane was added. The solid that formed was collected by filtration and dried under reduced pressure to give N-({[1-ethyl-1-(hydroxymethyl)propyl]amino}carbonothioyl)benzamide (7.1406 g, 80%) as a white solid, mp 161-163° C.; MS (ESI) m/z 281 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07618989B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-a8d2be81528f4cd6aee68e536b550742 |
| Source note | uspto-grants-2009_11 |