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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 22488Erstellt: 25. Oktober 2026

Hexane → 2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolane

https://huagongshe.com/reaction/22488

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHexaneHCID 8058—
Edukt5-Bromo-1,2,3-trimethoxybenzeneHCID 75885—
EduktMagnesium BromideHCID 82241—
Edukt2-(Benzenesulfonyl)-5-methoxyoxolaneHCID 19930462—
EduktButyllithiumHCID 178418339—
KatalysatorZinc bromideHCID 10421208—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-Methoxy-5-(3,4,5-trimethoxyphenyl)oxolaneHCID 1993045927,3%

Reaktionsschritte

To stirred solution of 1-bromo-3,4,5-trimethoxybenzene (2.47 g, 10 mmol) in THF (20 ml) at -78° C. was added 2.5M n-butyllithium in hexane (4.4 ml, 11 mmol). After 0.75 h the solution was cannulated into a mixture of 1M zinc(II) bromide in THF (11 ml, 11 mmol) and magnesium(II) bromide etherate (2.86 g, 15 mmol) in THF (10 ml) at -78° C. The resulting mixture was allowed to warm to room temperature over 1 h and then sonicated for 0.4 h. A solution of 2-benzenesulphonyl-5-methoxytetrahydrofuran (1.85 g, 7.5 mmol) in THF (10 ml)was added and the mixture stirred at room temperature for 1 h, sonicated for 1 h and stirred overnight. The reaction was quenched by the addition of aqueous ammonium chloride (20 ml). Work up and purification as described for Example 1(b) gave 2-(3,4,5-trimethoxyphenyl)-5 -methoxytetrahydrofuran (0.55 g, 27%) as a colourless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05428168
Quelldatensatzuspto-grants-1995_06
ORD IDord-ab76418b248b473985be7ed447798f4b
Quellennotizuspto-grants-1995_06