HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(Trimethylsilyl)furan-3-carbaldehyde → 3-(1-Hydroxytridecyl)-2-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15037165 | — |
| Reactant | HCID 178443215 | HCID 178443215 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(1-Hydroxytridecyl)-2-trimethylsilylfuran | HCID 15037168 | — |
Reaction Steps
A solution of dodecylmagnesium bromide (a 1M solution in tetrahydrofuran; 14.3 ml; 14.3 mmol) was added to a solution of 2-trimethylsilyl-3-furaldehyde (1.20 g, 7.1 mmol) in tetrahydrofuran (30 ml) at 0°. After all the aldehyde has reacted, as shown by tlc, the mixture was quenched with dilute hydrochloric acid and was extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave an oil, which was purified by a silica column using 5% ethyl ether/hexane to give the title furan.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322953 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-7b766b4a4bff426b9d1a8895b43975ff |
| Source note | uspto-grants-1994_06 |