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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 358243Generated: October 26, 2026

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

https://huagongshe.com/reaction/358243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthyl BromideHCID 6332—
ReactantPropyneHCID 6335—
ReactantMethyl phenylglyoxalateHCID 84835—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178419101HCID 178419101—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-hydroxy-2-phenylpent-3-ynoateHCID 271980—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04465834
Source datasetuspto-grants-1984_08
ORD IDord-cddf046e23764c22ab1722be07cde170
Source noteuspto-grants-1984_08