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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358242Erstellt: 25. Oktober 2026

Ethyl Bromide → Ethyl alpha-Phenyl-alpha-phenylethynylglycolate

https://huagongshe.com/reaction/358242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl BromideHCID 6332—
EduktPhenylacetyleneHCID 10821—
EduktEthyl benzoylformateHCID 15349—
EduktMagnesiumHCID 5462224—
EduktHCID 178418443HCID 178418443—
EduktHCID 178419644HCID 178419644—
LösungsmittelDiethyl EtherHCID 3283—
ProduktEthyl alpha-Phenyl-alpha-phenylethynylglycolateHCID 12328607—

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04465834
Quelldatensatzuspto-grants-1984_08
ORD IDord-eddc612bbc884e04842e80996f6a0f5b
Quellennotizuspto-grants-1984_08