HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dodecanal → 4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dodecanal | HCID 8194 | — |
| Reactant | 4-(4,4-Dibromo-3-butenyl)-2-triethylsilylfuran | HCID 15037105 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Hydroxy-3-hexadecynyl)-2-triethylsilylfuran | HCID 15037106 | — |
Reaction Steps
n-Butyl lithium (a 2.5M solution in tetrahydrofuran; 0.42 ml, 1.04 mmol) was added dropwise to a solution of 4-(4,4-dibromo-3-butenyl)-2-triethylsilylfuran (200 mg, 0.51 mmol) in tetrahydrofuran (8 ml) at -78° under argon. After 2 hours, a solution of 1-dodecanal (102 mg, 0.56 mmol) in tetrahydrofuran (1 ml) was added. Stirring was continued for 14 hours, while the cooling bath attained room temperature. The mixture was quenched with water and was extracted with ethyl ether. Evaporation of the dried (magnesium sulfate) extracts gave a residue, which was purified by a silica column with 15% ethyl ether/hexane to give the titled alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05059611 |
| Source dataset | uspto-grants-1991_10 |
| ORD ID | ord-c70f000417f641b2925d2d3d94cd306b |
| Source note | uspto-grants-1991_10 |