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HRID 358242作成日:2026年10月26日

Ethyl Bromide → Ethyl alpha-Phenyl-alpha-phenylethynylglycolate

https://huagongshe.com/reaction/358242

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl BromideHCID 6332—
反応物PhenylacetyleneHCID 10821—
反応物Ethyl benzoylformateHCID 15349—
反応物MagnesiumHCID 5462224—
反応物HCID 178418443HCID 178418443—
反応物HCID 178419644HCID 178419644—
溶媒Diethyl EtherHCID 3283—
生成物Ethyl alpha-Phenyl-alpha-phenylethynylglycolateHCID 12328607—

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04465834
出典データセットuspto-grants-1984_08
ORD IDord-eddc612bbc884e04842e80996f6a0f5b
出典メモuspto-grants-1984_08