HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium tert-butoxide → 1-Ethynyladamantane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Triethylene Glycol | HCID 8172 | — |
| Product | 1-Ethynyladamantane | HCID 594781 | — |
Reaction Steps
The Stetter and Goebel reference, also cited above, discloses the synthesis of 1-ethynyladamantane from 1-bromoadamantane in good yield. We repeated that procedure with minor modifications by reacting 1-bromoadamantane with vinyl bromide in the presence of aluminum bromide to give the 2,2-dibromoethyl derivative, then dehydrobrominating that derivative in situ with potassium t-butoxide in triethylene glycol to give 1-ethynyladamantane in 60% overall yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04918158 |
| Source dataset | uspto-grants-1990_04 |
| ORD ID | ord-e77a97c976974e468fb4e86195300586 |
| Source note | uspto-grants-1990_04 |