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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1294127Erstellt: 26. Oktober 2026

Water → Methyl 2-hydroxy-5-methoxybenzeneacetate

https://huagongshe.com/reaction/1294127

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktBenzyltrimethylammonium hydroxideHCID 66854—
EduktMethyl (methylsulfinyl)methyl sulfideHCID 99129—
Edukt5-Methoxy-2-(methoxymethoxy)benzaldehydeHCID 11435522—
LösungsmittelMethanolHCID 887—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 2-hydroxy-5-methoxybenzeneacetateHCID 1410424553%

Reaktionsschritte

A mixture of 5-methoxy-2-methoxymethoxybenzaldehyde (9.25 g), methyl methylthiomethyl sulfoxide (11.7 g), 40% solution of benzyltrimethylammonium hydroxide in methanol (10 mL) and tetrahydrofuran (200 mL) heated under reflux for 20 hrs. Water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated. A mixture of the obtained residue and 10% hydrogen chloride-methanol (80 mL) was heated under reflux for 15 hrs. The reaction mixture was concentrated, and ethyl acetate was added to the residue. The organic layer was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated. The obtained residue was subjected to silica gel column chromatography to give crystals (4.88 g, 53%) of methyl 2-(2-hydroxy-5-methoxyphenyl)acetate from a fraction eluted with ethyl acetate-hexane (1:4, v/v). Recrystallization from ethyl acetate-hexane gave colorless prism crystals. melting point: 69-70° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07238716B2
Quelldatensatzuspto-grants-2007_07
ORD IDord-060c2b2708234daeb7fc88b2f4334ef5
Quellennotizuspto-grants-2007_07