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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 472337Generated: October 27, 2026

Acetone → (4-((1,1-Dioxidothiomorpholino)methyl)phenyl)boronic acid

https://huagongshe.com/reaction/472337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)phenylboronic acidHCID 2735593—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
Product(4-((1,1-Dioxidothiomorpholino)methyl)phenyl)boronic acidHCID 54970580—

Reaction Conditions

Temperature40 °C

Reaction Steps

A suspension of (4-bromomethylphenyl)boronic acid (2.00 g, 9.31 mmol), thiomorpholine 1,1-dioxide (1.50 g, 11.1 mmol) and potassium carbonate (2.60 g, 18.8 mmol) in acetone (25 mL, 340 mmol) was heated at 40° C. for 18 hours then cooled to room temperature. The volatiles were evaporated and the residue was suspended in saturated aqueous ammonium chloride (100 mL). The aqueous was decanted from the waxy solid and the solid was dissolved in methanol (50 mL), filtered to remove insoluble salts and evaporated. 4-[(4-boronophenyl)methyl]-thiomorpholine 1,1-dioxide was isolated as a tan foam. The crude material was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633173B2
Source datasetuspto-grants-2014_01
ORD IDord-b976641f55424446aab7a54ccbcf9797
Source noteuspto-grants-2014_01