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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538638Generated: October 31, 2026

4-Bromo-1,1,1-trifluorobutane → 2-Methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/538638

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1,1,1-trifluorobutaneHCID 521006—
ReactantSodium MethoxideHCID 10942334—
ReactantEthyl 2-(acetylthio)-2-methylpropanoateHCID 57937863—
SolventEthanolHCID 702—
Product2-Methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl esterHCID 5925329084.3%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of 149 g (0.785 mol) of 2-acetylsulfanyl-2-methyl-propionic acid ethyl ester in EtOH (1.2 L, degassed under nitrogen for 1 h) are added 169.7 g (0.105 mol) of sodium methoxide, followed by a solution of 150 g (0.785 mol) of 4-bromo-1,1,1-trifluoro-butane. The reaction is heated to 85° C. for 3 d. The solvent is removed under reduced pressure. The residue is dissolved in DCM (1 L) and washed with saturated aq. NaHCO3 solution (2×1 L). The organic layer is dried over Na2SO4, filtered and the filtrate is concentrated under reduced pressure to afford 171 g of 2-methyl-2-(4,4,4-trifluoro-butylsulfanyl)-propionic acid ethyl ester. Yield: 84%; ESI-MS: 259 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865744B1
Source datasetuspto-grants-2014_10
ORD IDord-09be35502f674df1b33e3e0e7dcb1eef
Source noteuspto-grants-2014_10