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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761276Generated: October 31, 2026

Diethyl Sulfate → Ethyl trichloroacetate

https://huagongshe.com/reaction/1761276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl SulfateHCID 6163—
ReactantTrichloroacetic AcidHCID 6421—
ReactantDureneHCID 7269—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventWaterHCID 962—
ProductEthyl trichloroacetateHCID 10588—

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of trichloroacetic acid (3.33 g, 20 millimoles, Sigma, 99.0+%) in water (171.02 g) was introduced into a three-necked 500 mL flask and warmed up to 60° C. when mechanically stirred (600 rpm). Next, the organic phase consisting of diethyl sulfate (15.49 g, 100 millimoles, Aldrich, 99+%), Adogen 464 (0.90 g, 2 millimoles, Aldrich), and durene (chromatographic standard, 0.652 g, 5 millimoles. Aldrich, 98%) was added to the flask. The organic phase:aqueous phase weight ratio was 1:10. Since diethyl sulfate decomposes in water, the reaction mixture was stirred at 60° C. for 30 minutes. Then, the reaction was stopped and an aliquot of the organic phase was centrifuged to remove the aqueous phase and injected into the gas chromatographic column. The yield of ethyl trichloroacetate based on the limiting reactant (trichloroacetic acid) was 15%. No other products were present in the chromatogram.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846946B2
Source datasetuspto-grants-2005_01
ORD IDord-36e614d50b854e42b6e85a5ab87112bd
Source noteuspto-grants-2005_01