Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 358243Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktEthyl BromideHCID 6332—
EduktPropyneHCID 6335—
EduktMethyl phenylglyoxalateHCID 84835—
EduktMagnesiumHCID 5462224—
EduktHCID 178419101HCID 178419101—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 2-hydroxy-2-phenylpent-3-ynoateHCID 271980—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04465834
Quelldatensatzuspto-grants-1984_08
ORD IDord-cddf046e23764c22ab1722be07cde170
Quellennotizuspto-grants-1984_08