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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256210Generated: November 1, 2026

4-Fluorophenol → HCID 20164193, compound

https://huagongshe.com/reaction/256210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluorophenolHCID 9732—
ReactantHCID 20164211HCID 20164211—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 20164193HCID 20164193—

Reaction Steps

A solution of a p-fluorophenol in t-butanol is treated with one equivalent of potassium t-butoxide, followed by the compound of example 35A. The reaction mixture is then refluxed until all epoxide has reacted. The reaction is cooled, diluted with water, and extracted with ethyl acetate. The organic extracts are dried and concentrated. The carbobenzyloxy protecting group is removed by standard hydrogenolysis and the final product purified by chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04701461
Source datasetuspto-grants-1987_10
ORD IDord-586bd1bda8364275be67b853aaeca6c6
Source noteuspto-grants-1987_10