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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609637Generated: November 1, 2026

Diethyl Ether → 3-Fluoro-p-anisaldehyde

https://huagongshe.com/reaction/1609637

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantDichloromethaneHCID 6344—
Reactant2-FluoroanisoleHCID 67576—
CatalystTitanium TetrachlorideHCID 24193—
Product3-Fluoro-p-anisaldehydeHCID 67696—

Reaction Conditions

Temperature15 °C

Reaction Steps

To a solution of o-fluoroanisole, 101 g. (0.80 mole) in 500 ml. dry methylene chloride is added dropwise over 30 minutes a solution of titanium tetrachloride, 182 g. (0.96 mole, 1.2 equiv.) and α,α-dichloromethylmethyl ether, 110 g. (0.96 mole) in an equal volume of methylene chloride. The temperature is maintained at 10-20° C. with an ice-bath. The mixture is stirred at room temperature for 1 hour longer and then poured over crushed ice-water with stirring. Ether (1l.) is added, and the mixture stirred under nitrogen until solution occurs. The organic layer is extracted with water (3×), sodium bicarbonate solution (3×) and dried (MgSO4). The solvent is evaporated off at 30° to give crude product as an oil. The oil is vacuum distilled through a jacketed Vigreux column when it gives 3-fluoro-4-methoxybenzaldehyde, B.P. 120-121° C., at 10 mm. Hg; Rf 0.6 on a silica-gel G plate with methylene chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401774
Source datasetuspto-grants-1995_03
ORD IDord-d55cf4bbf69641488805a9fede514f95
Source noteuspto-grants-1995_03