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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538639Generated: October 29, 2026

Hydrochloric Acid → 2-Methyl-2-(3-methyl-butane-1-sulfonyl)-propionic acid

https://huagongshe.com/reaction/538639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium trimethylsilanolateHCID 23668039—
Reactant2-Methyl-2-(4,4,4-trifluoro-butane-1-sulfonyl)-propionic acid ethyl esterHCID 59253285—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-2-(3-methyl-butane-1-sulfonyl)-propionic acidHCID 59253211109%

Reaction Steps

To a solution of 170 g (0.59 mol) of 2-methyl-2-(4,4,4-trifluoro-butane-1-sulfonyl)-propionic acid ethyl ester in THF (3.4 L) are added 225.4 g (1.76 mol) of potassium trimethylsilanolate in portions over 0.5 h. The reaction is stirred at room temperature for 18 h. The reaction mixture is acidified with 2 M aq. HCl solution (2 L) to pH 2 and extracted with DCM (2×2 L). The combined organic extracts are dried (Na2SO4) and filtered. The filtrate is concentrated under reduced pressure to afford 143 g of 2-methyl-2-(3-methyl-butane-1-sulfonyl)-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865744B1
Source datasetuspto-grants-2014_10
ORD IDord-47f497e3014247a3a35ad09bbd1c39c4
Source noteuspto-grants-2014_10