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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 842332Erstellt: 25. Oktober 2026

Hydrochloric Acid → 1,3-Dihydroisobenzofuran

https://huagongshe.com/reaction/842332

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1,2-Bis(chloromethyl)benzeneHCID 11919—
Edukt1,2-BenzenedimethanolHCID 69153—
Edukt[2-(Chloromethyl)phenyl]methanolHCID 12416357—
Produkt1,3-DihydroisobenzofuranHCID 103272%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

A reagent, α,α′-dihydroxy-o-xylene, produced by Aldrich Co. (69.5 g, 0.5 mol) was placed in a 500-mL four-neck flask equipped with a condenser tube, a stirring blade, a thermometer, and a dropping funnel, and 35% hydrochloric acid (100 g, 1.0 mol) was added thereto. The mixture was stirred at 70° C. for one hour. After completion of reaction, the reaction mixture was allowed to stand, so that two-separated layers were formed. The reaction was analyzed through GC while stirring again during sampling. From the obtained concentration of α-chloro-α′-hydroxy-o-xylene, the yield of α-chloro-α′-hydroxy-o-xylene was calculated to be 91% based on α,α′-dihydroxy-o-xylene. The conversion of α,α′-dihydroxy-o-xylene was 99%, and α,α′-dichloro-o-xylene (5%) and phthalan (2%) were formed as by-products.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06372921B1
Quelldatensatzuspto-grants-2002_04
ORD IDord-e5cb971104e741ab8a3c6cc2047f7110
Quellennotizuspto-grants-2002_04