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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647902Erstellt: 25. Oktober 2026

Hydrochloric Acid → Ethyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoate

https://huagongshe.com/reaction/647902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium IodideHCID 5238—
EduktSodium hydrideHCID 24758—
EduktEthyl 5-bromovalerateHCID 84580—
EduktMethyl 2,4-dihydroxy-3-formylbenzoateHCID 4413713—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoateHCID 2048434742%

Reaktionsschritte

Methyl 2,4-dihydroxy-3-formylbenzoate (10.0 g, 0.051 M) was added to dimethylformamide (100 ml), then to this mixture was added sodium hydride (1.344 g, 0.056 M), portionwise. The mixture became warm and effervescence occurred. When the addition was complete the reaction mixture was left to stir at room temperature for 10 minutes. To this solution was then added sodium iodide (0.765 g), ethyl 5-bromovalerate (11.7 g, 0.056 M), and a further 20 ml of dimethylformamide. The whole was brought to 60° C. and left to stir for 5 days. The reaction mixture was cooled, poured into water (200 ml), acidified with concentrated hydrochloric acid, and extracted into ethyl acetate (2×75 ml). The combined organic layers were washed with water (2×75 ml), 5% sodium hydroxide solution (50 ml), water (50 ml) and brine (50 ml), dried (magnesium sulphate), filtered and the solvent removed in vacuo to give ethyl 5-(2-formyl-3-hydroxy-4-methoxycarbonylphenoxy)pentanoate 6.92 g, 42% as a yellow oil, purified by column chromatography and obtained as a pale-yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04410537
Quelldatensatzuspto-grants-1983_10
ORD IDord-547556c0c1344c01adf5f7a7d54a07e2
Quellennotizuspto-grants-1983_10