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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1248873Generated: October 30, 2026

1,3-Dioxolane, 2-(4-fluoro-3-phenoxyphenyl)- → 4-Fluoro-3-phenoxybenzaldehyde

https://huagongshe.com/reaction/1248873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dioxolane, 2-(4-fluoro-3-phenoxyphenyl)-HCID 11970646—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Fluoro-3-phenoxybenzaldehydeHCID 11006891%

Reaction Steps

A solution of 26 g (0.1 mol) of 4-fluoro-3-phenoxy-benzaldehyde ethyleneacetal in 60 ml of ethanol, 20 ml of water and 1 ml of concentrated hydrochloric acid was stored at room temperature for 3 hours. The ethanol was then distilled off in vacuo, and 100 ml of toluene were added to the residue. The water was separated off and the organic phase was washed twice with 50 ml of water each time, dried over sodium sulphate and evaporated in vacuo. The residue was distilled in vacuo. 19.6 g (91% of theory) of 4-fluoro-3-phenoxy-benzaldehyde were obtained in this manner in the form of a colorless oil with a boiling point of 102°-104° C./0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04626601
Source datasetuspto-grants-1986_12
ORD IDord-7c0782b66eed4a66ac8f677b6a564ab3
Source noteuspto-grants-1986_12