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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266867Generated: October 30, 2026

Sodium Thiosulfate → 4,4,4-Trifluoro-2-methylbutanal

https://huagongshe.com/reaction/2266867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
Reactant4,4,4-Trifluoro-2-methylbutan-1-olHCID 2775532—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product4,4,4-Trifluoro-2-methylbutanalHCID 7434999288%

Reaction Conditions

Temperature25 °C

Reaction Steps

To 2-methyl-4,4,4-trifluoro-1-butanol (7.5 g, 53 mmol) in methylene chloride (CH2Cl2) (125 mL) at 0° C. was added Dess-Martin periodinane (26.5 g, 63.3 mmol). The reaction mixture was warmed to 25° C. and stirred for 20 min. To this mixture was added diethyl ether (Et2O—200 mL) followed by a solution of Na2S2O3 (29.0 g, 185 mmol) in a saturated aqueous solution of sodium bicarbonate (NaHCO3) (200 mL) and 100 mL of water. The milky white mixture was stirred until both phases were homogeneous. The phases were separated and the organic extract was washed with saturated aqueous NaHCO3 (25 mL) and aqueous 1 N Na2S2O3 (25 mL) and dried using magnesium sulfate (MgSO4). Solvents were removed by distillation at atmospheric pressure to give 2-methyl-4,4,4-trifluorobutanal (6.5 g, 88%). 1H nuclear magnetic resonance (NMR) spectrum matched that which was reported in the literature (J. Fluorine Chem. 36: 163-170 (1987).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858658B2
Source datasetuspto-grants-2010_12
ORD IDord-bc19b7b8c9654000aa3d711aca09e981
Source noteuspto-grants-2010_12