HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-[1-(Acetamido)tridecyl]-5-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(1-Aminotridecyl)-5-trimethylsilylfuran | HCID 15037077 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-[1-(Acetamido)tridecyl]-5-trimethylsilylfuran | HCID 15037078 | — |
Reaction Steps
Acetic anhydride (0.1 ml) was added to a solution of 3-(1-aminotridecyl)-5-trimethylsilylfuran (89.8 mg, 0.27 mmol) and triethylamine (0.1 ml) in dichloromethane (1 ml) at room temperature. Stirring was continued overnight (14 hours) while the cooling bath attained room temperature. The residue, after solvent removal, was purified by preparative TLC (20×20 cm, 1000u; developed with 60% ethyl ether/hexane). The title amide was obtained as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05298633 |
| Source dataset | uspto-grants-1994_03 |
| ORD ID | ord-c22b1edad787426a833a06de04e35160 |
| Source note | uspto-grants-1994_03 |