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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1609402Erstellt: 23. Oktober 2026

Hydrogen iodide → Orcinol

https://huagongshe.com/de/reaction/1609402

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen iodideHCID 24841—
Edukt3,5-DimethoxytolueneHCID 77844—
ProduktOrcinolHCID 10436—

Reaktionsschritte

Methylmagnesium bromide (35 g) was added to 1,3-dimethoxy-5-benzoyl chloride (100 g) to obtain 1,3-dimethoxy-methylphenone in a yield of 45%. Then, the reduction was conducted by adding water (300 cc), concentrated hydrochloric acid (300 cc) and 1,3-dimethoxy-methylphenone (100 g) to zinc amalgam obtained from zinc (400 g) and mercuric chloride (20 g). Further, concentrated hydrochloric acid (10 to 15 cc) was added every one hour. After the completion of the reaction, the reaction solution was cooled and saturated with sodium chloride, and then extracted with ether to obtain 40 g of 1,3-dimethoxy-5-methylbenzene. Hydrogen iodide was added to the resulting 1,3-dimethoxy-5-methylbenzene and stirred at 115° to 125° C. for 3 hours under nitrogen atmosphere. After cooling, the product was extracted with methylene chloride to obtain 30 g of 5-methylresorcinol.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05399785
Quelldatensatzuspto-grants-1995_03
ORD IDord-95315044872d4612af294f918464c28a
Quellennotizuspto-grants-1995_03