HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Bis-[(2-triethylsilyl-4-furyl)methyl]oxalate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 4-Hydroxymethyl-2-triethylsilylfuran | HCID 15037035 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Bis-[(2-triethylsilyl-4-furyl)methyl]oxalate | HCID 15037121 | — |
Reaction Steps
Oxalyl chloride (0.59 ml, 6.79 mmol) was added dropwise to a solution of 4-hydroxymethyl-2-triethylsilylfuran (Compound 1, 1.2 g, 5.66 mmol) and triethylamine (0.95 ml, 6.79 mmol) in dichloromethane (10 ml) at 0°. After 10 minutes, the reaction mixture was quenched with ice. Extraction (dichloromethane) and evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by flash chromatography on silica using 5% ethyl ether/hexane. Fractions with Rf of about 0.17 gave, after evaporation the title oxalate ester 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-f8016cc81bfd41548b2e81d770fabd5f |
| Source note | uspto-grants-1994_03 |