HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15037082, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 3-(1-Aminotridecyl)-5-trimethylsilylfuran | HCID 15037077 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15037082 | HCID 15037082 | — |
Reaction Steps
Methanesulfonyl chloride (37 μl, 0.48 mmol) was added to a solution of 3-(1-aminotridecyl)-5-trimethylsilylfuran (134.6 mg, 0.4 mmol) and triethylamine (67 μl, 0.48 mmol) in dichloromethane (2 ml) at 0°. Stirring continued overnight (14 hours) while the cooling both attained room temperature. The reaction mixture was quenched with water. Extraction (ethyl ether) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 10% ethyl ether/hexane. Fractions with Rf of about 0.07 on evaporation gave the title sulfonamide as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05089485 |
| Source dataset | uspto-grants-1992_02 |
| ORD ID | ord-7481f22f8a1b49d5ab74b1515c6c9c2d |
| Source note | uspto-grants-1992_02 |