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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358242Generated: October 23, 2026

Ethyl Bromide → Ethyl alpha-Phenyl-alpha-phenylethynylglycolate

https://huagongshe.com/en/reaction/358242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantPhenylacetyleneHCID 10821—
ReactantEthyl benzoylformateHCID 15349—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178418443HCID 178418443—
ReactantHCID 178419644HCID 178419644—
SolventDiethyl EtherHCID 3283—
ProductEthyl alpha-Phenyl-alpha-phenylethynylglycolateHCID 12328607—

Reaction Steps

A solution of phenylacetylene (11.2 g., 0.1 mole) in 25 ml. of anhydrous ether was added over a 45 minute period to a suspension of ethylmagnesium bromide (0.1 mole) prepared from magnesium (2.4 g., 0.1 g. atom) and ethyl bromide (10.9 g., 0.1 mole) in 100 ml. of ether. The mixture was stirred overnight. The resultant phenylethynylmagnesium bromide suspension was subsequently added dropwise through a stop-cock at the base of the flask to a solution of ethyl phenylglyoxylate (17.8 g., 0.1 mole) in 100 ml. of dry ether at 0°-5° over a two hour period. The cooling bath was removed and the mixture stirred for five hours. The reaction mixture was kept overnight, then poured on a slurry of ice and concentrated hydrochloric acid and extracted with ether. The ether extracts were dried and the solvent distilled in vacuo. The resultant oil was distilled to give 14.5 g. (52%) of product, b.p. 170°-82° (0.25 mm.). An analytical sample distilled at 156°-58° (0.08 mm.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465834
Source datasetuspto-grants-1984_08
ORD IDord-eddc612bbc884e04842e80996f6a0f5b
Source noteuspto-grants-1984_08