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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873935Generated: November 2, 2026

Hydrochloric Acid → HCID 12691335, compound

https://huagongshe.com/reaction/1873935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,3,5-TribromobenzeneHCID 12279—
ReactantHexafluoroacetoneHCID 12695—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductHCID 12691335HCID 1269133560.2%

Reaction Conditions

Temperature-78 °C

Reaction Steps

Under nitrogen atmosphere, a 500 mL glass flask was charged with 30.0 g (95.0 mmol) of 1,3,5-tribromobenzene and 400 mL of diethyl ether, followed by cooling to −78° C. At −78° C., 60 mL of a 1.6M solution containing 96.0 mmol of n-butyllithium in hexane was added dropwise by spending 1 hr, followed by aging at −78° C. for 1 hr. After confirming lithiation by gas chromatography, 16.6 g (100.0 mmol) of hexafluoroacetone was bubbled at −78° C., followed by stirring for 1 hr. After stirring, the reaction liquid was added to 400 mL of 2N hydrochloric acid to separate it into an organic layer and an aqueous layer. The aqueous layer was extracted with 100 mL of isopropyl ether. The combined organic layer was dried with anhydrous magnesium sulfate, followed by concentration with an evaporator and then solid distillation, thereby obtaining 23.0 g of 1-[2,2,2-trifluoro-1-hydroxy-1-(trifluoromethyl)ethyl]-3,5-dibromobenzene (yield: 60%) represented by the following formula.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304508B2
Source datasetuspto-grants-2012_11
ORD IDord-9545244e3be248c1896cbf745dbd4bfb
Source noteuspto-grants-2012_11