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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 851286Erstellt: 25. Oktober 2026

Methanol → 2-Bromo-4-(dimethoxymethyl)-1-fluorobenzene

https://huagongshe.com/reaction/851286

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethanolHCID 887—
EduktTrimethyl orthoformateHCID 9005—
Edukt3-Bromo-4-fluorobenzonitrileHCID 123579—
KatalysatorNickelHCID 935—
LösungsmittelFormic AcidHCID 284—
LösungsmittelWaterHCID 962—
Produkt2-Bromo-4-(dimethoxymethyl)-1-fluorobenzeneHCID 2226086475%

Reaktionsschritte

A mixture of 85 g of Raney nickel, which had been washed thoroughly with water, 500 ml of formic acid and 100 g (0.5 mole) of 3-bromo-4-fluoro-benzonitrile was stirred for 24 hours at 90°-100° C. under an atmosphere of a blanketing gas (nitrogen or argon). After cooling to room temperature, 1 liter of water was added and the mixture was extracted twice with 300 ml of toluene. The combined toluene solutions were washed with 200 ml of water, with 200 ml of saturated sodium bicarbonate solution and again with 200 ml of water and then dried by incipient distillation. 1.5 g of air-dried ion exchanger SPC 118, 16 g (0.5 mole) of methanol and 58.5 g (0.55 mole) of orthoformic acid trimethyl ester were then added to the solution, the mixture was stirred for a further 1 hour without a bath and was then warmed at 50° C. for 2 hours. The reaction mixture was cooled, filtered to remove the ion exchanger and washed with 200 ml of 5% strength potassium carbonate solution. The solvent was then stripped off and the residue was distilled in vacuo. 93 g (75% of theory) of 3-bromo-4-fluoro-benzaldehyde dimethyl acetal were obtained in this way, in the form of a colorless liquid with a boiling point of 67°-68° C./0.1 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04383949
Quelldatensatzuspto-grants-1983_05
ORD IDord-04dc028d0ccc418897fc25f96e9ef5a1
Quellennotizuspto-grants-1983_05