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HRID 358243作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ethyl BromideHCID 6332—
反応物PropyneHCID 6335—
反応物Methyl phenylglyoxalateHCID 84835—
反応物MagnesiumHCID 5462224—
反応物HCID 178419101HCID 178419101—
溶媒Diethyl EtherHCID 3283—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 2-hydroxy-2-phenylpent-3-ynoateHCID 271980—

反応手順

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.

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-cddf046e23764c22ab1722be07cde170
出典メモuspto-grants-1984_08