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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant(+-)-3-QuinuclidinolHCID 15381—
ReactantSodiumHCID 5360545—
ReactantEthyl alpha-cyclopentyl-alpha-phenylethynylglycolateHCID 54429989—
SolventHexaneHCID 8058—
Product3-Quinuclidyl alpha-Cyclopentyl-alpha-phenylethynylglycolateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465834
Source datasetuspto-grants-1984_08
ORD IDord-a5ffa85c4f634c8b88558d41d700b285
Source noteuspto-grants-1984_08