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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 576054Generated: October 23, 2026

Sodium Thiosulfate → 2-(4-Tert-butylphenyl)acetaldehyde

https://huagongshe.com/en/reaction/576054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantp-tert-Butylphenethyl alcoholHCID 79410—
ReactantTriacetoxyperiodinaneHCID 159087—
SolventChloroformHCID 6212—
Product2-(4-Tert-butylphenyl)acetaldehydeHCID 59534080.2%

Reaction Steps

A solution of 2-(4-tert-butylphenyl)ethanol (5.35 g, 30.0 mmol) in chloroform (150 mL) was cooled in ice and Dess-Martin periodinane (16.5 g, 39.0 mmol) was added thereto. The mixture was warmed to room temperature and stirred for 3 hr. The reaction mixture was diluted with chloroform (150 mL), followed by cooling in ice. Thereafter, saturated aqueous sodium thiosulfate solution was added thereto and the mixture was stirred for 5 min. The mixture was extracted three times with chloroform and then the organic layer was washed with brine and dried over anhydrous magnesium sulfate. The desiccant was filtered off and then the filtrate was concentrated under reduced pressure. The resulting precipitate was filtered again, followed by washing with chloroform. The filtrate was concentrated under reduced pressure and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1) to afford the title compound as a yellow oil (4.24 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09035059B2
Source datasetuspto-grants-2015_05
ORD IDord-2074c7fe8f0340458aeb70fe936da491
Source noteuspto-grants-2015_05