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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608926Generated: November 2, 2026

Water → 2-Fluoro-4-(4-chlorophenylmethoxy)aniline

https://huagongshe.com/reaction/1608926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Fluoro-4-(4-chlorophenylmethoxy)nitrobenzeneHCID 20083075—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
Product2-Fluoro-4-(4-chlorophenylmethoxy)anilineHCID 2124985088.2%

Reaction Conditions

Temperature25 °C

Reaction Steps

A stirred solution of 9.0 grams (0.032 mole) of 2-fluoro-4-(4-chlorophenylmethoxy)nitrobenzene and 10 mL of water in 150 mL of glacial acetic acid was maintained at 50° C. while 9.0 grams of iron powder was slowly added. Upon completion of addition, the reaction mixture was cooled to 25° C. where it was stirred for about one hour. After this time the reaction mixture was filtered ,and the filtrate was poured into water. The mixture was then extracted with ethyl acetate. The extract was dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to a residue. The residue was subjected to column chromatography using silica gel. Elution was accomplished using methylene chloride. The product-containing fractions were combined and concentrated under reduced pressure, yielding 7.1 grams of 2-fluoro-4-(4-chlorophenylmethoxy)aniline, mp 73°-75° C. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399543
Source datasetuspto-grants-1995_03
ORD IDord-6b7c6904ff5c4329affc8da9ecd381d7
Source noteuspto-grants-1995_03