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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2246759Erstellt: 27. Oktober 2026

Hydrochloric Acid → 4-Hexyl-2-methoxy-1-phenoxybenzene

https://huagongshe.com/reaction/2246759

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Chloro-2-methoxy-1-phenoxybenzeneHCID 58604131—
EduktHCID 178444611HCID 178444611—
KatalysatorZincchlorideHCID 3007855—
KatalysatorHCID 178418851HCID 178418851—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt4-Hexyl-2-methoxy-1-phenoxybenzeneHCID 68425585—

Reaktionsschritte

Under nitrogen, ZnCl2 (0.5 M solution in tetrahydrofuran; 6.8 mL, 3.41 mmol) was added by syringe to a round-bottomed flask sealed with a rubber septum and purged with nitrogen. Hexyl magnesium chloride (1.0 M solution in THF; 4.0 mL, 4.26 mmol) was then added dropwise by syringe, and the resulting solution was stirred at room temperature for 20 minutes. Next, N-methylpyrrolidinone (4.7 mL) was added by syringe. After 5 minutes, 21.7 mg (0.0426 mmol) Pd(P(t-Bu)3)2 and 500 mg (2.13 mmol) of compound (3) were added. The flask was then fitted with a reflux condenser and heated under refluxed for 48 hours. The flask was then gradually cooled to room temperature, and 20 mL of a 1.0M aqueous HCl solution was added. The resulting mixture was extracted with diethyl ether and the ether extract was washed with water, then dried over anhydrous MgSO4 and concentrated under vacuum to give the crude product. Purification by flash chromatography on silica gel afforded analytically pure compound (4a): 1H NMR (300 MHz) (CDCl3): δ 7.36-6.80 (m, 8H), 3.90 (s, 3H), 2.71-2.66 (t, 2H), 1.74-1.67 (m, 2H), 1.42-1.33 (m, 6H), 1.01-0.97 (t, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07687547B2
Quelldatensatzuspto-grants-2010_03
ORD IDord-12a50118fbf5444c8e6902f424180700
Quellennotizuspto-grants-2010_03