HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylene → 6-Cyclopentylidene-3-methylhex-1-yn-3-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | 5-Cyclopentylidenepentan-2-one | HCID 13528013 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Cyclopentylidene-3-methylhex-1-yn-3-ol | HCID 18433852 | 81% |
Reaction Steps
Acetylene was bubbled for 50 minutes through a solution of tBuOK (33.8 g; 0.30 mol) in THF (240 ml) at 0° C. The resulting beige suspension was treated with 5-cyclopentylidenepentan-2-one (41.7 g; 0.27 mol) added dropwise for 15 minutes at 0° C. The resulting mixture was warmed gently to room temperature and quenched with saturated NH4Cl (180 ml). The aqueous phase was separated and extracted with MTBE (2×120 ml). The combined organic layers were washed with H2O (240 ml), brine (100 ml), dried over MgSO4, and concentrated in vacuo. Distillation (69° C.-71° C./0.09 torr) afforded 38.95 g (81% yield) of 6-cyclopentylidene-3-methylhex-1-yn-3-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06399811B1 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-d457b3ff82a24073bb695f55caf34eed |
| Source note | uspto-grants-2002_06 |