HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358249Generated: October 29, 2026
Toluene → 3-Quinuclidyl alpha-Cyclopentyl-alpha-phenylethynylglycolate
https://huagongshe.com/reaction/358249
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (+-)-3-Quinuclidinol | HCID 15381 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Ethyl alpha-cyclopentyl-alpha-phenylethynylglycolate | HCID 54429989 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Quinuclidyl alpha-Cyclopentyl-alpha-phenylethynylglycolate | HCID 13371147 | — |
Reaction Steps
3-Quinuclidinol (3.8 g., 0.030 mole) and about 0.05 g. of sodium were refluxed in 50 ml. of toluene, in a flask equipped with a reflux head, until all the sodium reacted. Then, ethyl α-cyclopentyl-α-phenylethynylglycolate (5.4 g., 0.02 mole) in 35 ml. of solvent was added dropwise over an hour period. No temperature drop was noted in the reflux head. The reaction mixture was refluxed for about 18 hours and then about 40 ml. of solvent was distilled from the reaction flask over a four hour period. The reaction mixture was cooled, and dry 20°-40° petroleum ether was added. A tarry solid formed and was filtered. The solid was treated with hot hexane to yield 3.2 g. (45%) of crude product melting about 115° C. The pure compound, m.p. 137°-39°, was obtained by recrystallization from hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04465834 |
|---|
| Source dataset | uspto-grants-1984_08 |
|---|
| ORD ID | ord-a5ffa85c4f634c8b88558d41d700b285 |
|---|
| Source note | uspto-grants-1984_08 |
|---|