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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485070Generated: October 31, 2026

Sodium Thiosulfate → 2-(3-(Trifluoromethyl)phenyl)acetaldehyde

https://huagongshe.com/reaction/1485070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant3-(Trifluoromethyl)phenethylic alcoholHCID 95926—
ReactantTriacetoxyperiodinaneHCID 159087—
ReactantSodium BicarbonateHCID 516892—
SolventChloroformHCID 6212—
Product2-(3-(Trifluoromethyl)phenyl)acetaldehydeHCID 2124633960.1%

Reaction Steps

To a solution of 3-(trifluoromethyl)phenethyl alcohol (2.00 g) in chloroform (50.0 mL), Dess-Martin periodinane (4.70 g) was added under cooling with ice. After being brought to room temperature, the reaction mixture was stirred for an hour. Subsequently, a saturated aqueous solution of sodium hydrogencarbonate (25.0 mL) and a saturated aqueous solution of sodium thiosulfate (25.0 mL) were added and the mixture was vigorously stirred for an hour. After phase separation, the organic layer was dried over anhydrous magnesium sulfate, the desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=98:2-85:15) to give the titled compound as a pale yellow oil (1.19 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422240B2
Source datasetuspto-grants-2016_08
ORD IDord-5499289300934ec392cbbf0a12edf137
Source noteuspto-grants-2016_08