HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Acetate hexane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 3-(1-Aminotridecyl)-5-trimethylsilylfuran | HCID 15037077 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetate hexane | HCID 22139250 | — |
| Product | 3-[(N-methylureido)tridecyl]-5-Trimethylsilylfuran | HCID 54351178 | — |
Reaction Steps
A solution of methylisocyanate (23ul, 0.38 mmol) in dichloromethane (0.5 ml) was added to a solution of 3-(1-aminotridecyl)-5-trimethylsilylfuran (85.5 mg, 0.25 mmol) and triethylamine (53 microliter, 0.3 mmol) in dichloromethane (2 ml) at room temperature. Stirring was continued for two days and the reaction mixture was quenched with water. Extraction (dichloromethane) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by preparative TLC (20×20 CM, 1000ul; developed with 40% ethyl acetate/hexane) to give the titled urea as acetate/hexane) to give the titled urea as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298633 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-cf47fff7e2564292b5b5a8973c6486b1 |
| Source note | uspto-grants-1994_03 |