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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400631Generated: October 26, 2026

Water → 1-(1-Fluorocyclopropyl)-3-(5-fluoro-2-methoxyphenyl)-3-methylbutan-1-ol

https://huagongshe.com/reaction/400631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiiodomethaneHCID 6346—
Reactant2-Fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-olHCID 60026610—
ReactantHCID 178418750HCID 178418750—
SolventEthyl AcetateHCID 8857—
Product1-(1-Fluorocyclopropyl)-3-(5-fluoro-2-methoxyphenyl)-3-methylbutan-1-olHCID 60026339—

Reaction Steps

To 2-fluoro-5-(5-fluoro-2-methoxyphenyl)-5-methylhex-1-en-3-ol, stirred under nitrogen gas and cooled on ice, was added 8.0 mL of diethyl zinc (1.1 M in toluene). After 5 minutes, 1.0 mL of diiodomethane was added dropwise over 20 minutes, and the mixture was stirred and allowed to come to room temperature and then stirred at room temperature for 2 days. Then 0.5 mL of water was added, followed by ethyl acetate, and the mixture was filtered through diatomaceous earth. The product was concentrated in vacuo and the residue was fractionated over silica gel (hexanes-dichloromethane (1:1) to dichloromethane, gradient) to give 0.8 g of 1-(1-fluorocyclopropyl)-3-(5-fluoro-2-methoxyphenyl)-3-methylbutan-1-ol as an oil which was used without additional purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741897B2
Source datasetuspto-grants-2014_06
ORD IDord-a38a94b49db64afab6715a1ae93563cd
Source noteuspto-grants-2014_06