HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-(1-Acetoxytridecyl)-2-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15037165 | — |
| Reactant | HCID 178443215 | HCID 178443215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-Acetoxytridecyl)-2-trimethylsilylfuran | HCID 15037142 | — |
Reaction Steps
Dodecylmagnesium bromide (a 1.0 M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added to a solution 2-trimethylsilyl-3-furaldehyde (Compound 12, 1.20 g, 7.1 mmol) in tetrahydrofuran (20 ml). When all the aldehyde was consumed, as monitored by tlc, acetic anhydride (2.02 ml, 21.4 mmol) was added. Stirring was continued at room temperature for 14 hours. The mixture was quenched with water and was extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by a silica column using 2% ethyl ether/hexane to give the titled furan.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05043457 |
| Source dataset | uspto-grants-1991_08 |
| ORD ID | ord-405661060c3e4ff19646f072d5b00997 |
| Source note | uspto-grants-1991_08 |