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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249528Generated: October 31, 2026

4-Fluorophenol → HCID 20164193, compound

https://huagongshe.com/reaction/1249528

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 numberUS04632929
Source datasetuspto-grants-1986_12
ORD IDord-34420be20bb0476986b54249c5407f2f
Source noteuspto-grants-1986_12