HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetylene → 2-Ethynyldecahydronaphthalen-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetylene | HCID 6326 | — |
| Reactant | 2-Decalone | HCID 100328 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Ethynyldecahydronaphthalen-2-ol | HCID 21261618 | 86% |
Reaction Steps
Acetylene was bubbled for 4 hours through a mixture of tBuOK (95.8 g, 0.85 mol) in THF (11) at 0° C. 2-Decalone (100 g, 0,66 mol) was added slowly at RT to the slightly yellow suspension and the resulting mixture was stirred for additional 3.5 hours, quenched with saturated NH4Cl (500 ml) solution, and extracted with MTBE (2×700 ml). The combined organic phases were washed with NH4Cl (500 ml), H2O (2×500 ml), saturated NaCl (500 ml) solution until neutral pH was achieved, dried (MgSO4), and concentrated in vacuo. The crude orange oil was flash distilled (0.01 Torr, 88-90° C.) yielding 100.6 g (86%) of 2-ethynyldecahydro-naphthalen-2-ol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06184419B2 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-a157331c8c8b47179dfdbd0bcf7692ea |
| Source note | uspto-grants-2001_02 |