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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 358243생성일: 2026년 10월 23일

Hydrochloric Acid → Methyl 2-hydroxy-2-phenylpent-3-ynoate

https://huagongshe.com/ko/reaction/358243

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Ethyl BromideHCID 6332—
반응물PropyneHCID 6335—
반응물Methyl phenylglyoxalateHCID 84835—
반응물MagnesiumHCID 5462224—
반응물HCID 178419101HCID 178419101—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
생성물Methyl 2-hydroxy-2-phenylpent-3-ynoateHCID 271980—

반응 단계

1-Propynylmagnesium bromide (0.2 mole) was made from magnesium (4.8 g., 0.2 g. atom) ethyl bromide (21.8 g., 0.2 mole) and excess propyne gas in 400 ml. of THF. The Grignard reagent then was siphoned under nitrogen into an addition funnel and added dropwise over a 40 minute period to a cooled solution of methyl phenylglyoxylate (32.8 g., 0.2 mole) in 200 ml. of THF. A slight temperature rise took place. The reaction mixture was stirred for 24 hours, and then poured onto a slurry of ice and 25 ml. conc. HCl. Ether was added, and the layers were separated. Several more ether extracts were made and the organic extracts combined and dried. The volatile components were stripped subsequently in vacuo and the residue distilled to yield 13.1 g. (32%) of the product, b.p. 109°-12° (0.2 mm.). The oil solidified on standing and melted at 64°-65° after recrystallization from 20°-40° petroleum ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04465834
출처 데이터셋uspto-grants-1984_08
ORD IDord-cddf046e23764c22ab1722be07cde170
출처 메모uspto-grants-1984_08