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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920161Generated: October 29, 2026

Trifluoroacetic acid → (R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-1,1-dioxo-1lambda6-thiomorpholin-3-one

https://huagongshe.com/reaction/920161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
Reactant(R)-5-(5-bromo-2-fluoro-phenyl)-4-(2,4-dimethoxy-benzyl)-5-methyl-1,1-dioxo-1lambda6-thiomorpholin-3-oneHCID 90067087—
Product(R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-1,1-dioxo-1lambda6-thiomorpholin-3-oneHCID 9006709766.9%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of (R)-5-(5-bromo-2-fluoro-phenyl)-4-(2,4-dimethoxy-benzyl)-5-methyl-1,1-dioxo-1λ6-thiomorpholin-3-one (251 mg, 516 μmol, Eq: 1.00) and trifluoroacetic acid (5.88 g, 3.98 ml, 51.6 mmol, Eq: 100) was stirred at 23° C. for 16 hours. Poured into 1 M Na2CO3-sol. and extracted twice with ethyl acetate. The combined organic layers were dried over Na2SO4, filtered and evaporated. The residue was chromatographed on 5 g silica gel with dichloromethane/ethyl acetate 9:1 to give (R)-5-(5-bromo-2-fluoro-phenyl)-5-methyl-1,1-dioxo-1λ6-thiomorpholin-3-one (116 mg, 345 μmol, 66.9% yield) as a white solid. MS (ISN): m/z=334.0 [M−H]− and 336.0 [M+2−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273042B2
Source datasetuspto-grants-2016_03
ORD IDord-d8ecc100eb2a4111be10463de92d3415
Source noteuspto-grants-2016_03