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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358242생성일: 2026년 10월 26일

Ethyl Bromide → Ethyl alpha-Phenyl-alpha-phenylethynylglycolate

https://huagongshe.com/reaction/358242

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl BromideHCID 6332—
반응물PhenylacetyleneHCID 10821—
반응물Ethyl benzoylformateHCID 15349—
반응물MagnesiumHCID 5462224—
반응물HCID 178418443HCID 178418443—
반응물HCID 178419644HCID 178419644—
용매Diethyl EtherHCID 3283—
생성물Ethyl alpha-Phenyl-alpha-phenylethynylglycolateHCID 12328607—

반응 단계

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.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04465834
출처 데이터셋uspto-grants-1984_08
ORD IDord-eddc612bbc884e04842e80996f6a0f5b
출처 메모uspto-grants-1984_08