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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741684Generated: October 25, 2026

tert-Butanol → 1-(4-Fluorophenyl)-2-(4-(methylsulfonyl)phenyl)ethanol

https://huagongshe.com/reaction/741684

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant1-(4-Fluorophenyl)-2-(4-(methylthio)phenyl)ethanolHCID 19426792—
ReactantPotassium hydroxy sulfiteHCID 23707502—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-(4-Fluorophenyl)-2-(4-(methylsulfonyl)phenyl)ethanolHCID 19426795—

Reaction Steps

To a suspension of the product of step 1 (42 g, 160 mmol) in a mixture of CH2Cl2 (200 mL), t-BuOH (500 mL) was added a suspension of oxone (144 g, 234 mmol) in 1 L of H2O. The mixture was stirred for 72 h. CH2Cl2 was added until all solid dissolved. The resulting mixture was extracted with EtOAc. The organic extracts were dried (Na2SO4) and concentrated to give 47 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552422
Source datasetuspto-grants-1996_09
ORD IDord-cb8ba6c4bdaf417590451d616c8a1520
Source noteuspto-grants-1996_09