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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217505Generated: October 31, 2026

Sodium Hydroxide → 3-(Methylthio)-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/217505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant[3-(Methylthio)-5-(trifluoromethyl)phenyl]methanolHCID 68687257—
SolventDichloromethaneHCID 6344—
Product3-(Methylthio)-5-(trifluoromethyl)benzaldehydeHCID 59343879—

Reaction Steps

A solution of [3-(methylthio)-5-(trifluoromethyl)phenyl]methanol (200 mg, 0.99 mmol) in CH2Cl2 (20 mL) was cooled to 0° C. and then Dess-Martin periodinane (573 mg, 1.35 mmol) was added. The reaction was slowly warmed to room temperature. After stirring at room temperature for twenty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (75 mL). The organic extracts were washed with brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 1% to 10% EtOAc/hexanes afforded 3-(methylthio)-5-(trifluoromethyl)benzaldehyde. Rf=0.55 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 7.87 (s, 1H), 7.84 (s, 1H), 7.68 (s, 1H), 2.58 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193365B2
Source datasetuspto-grants-2012_06
ORD IDord-a44bb186049b47e3ad92d1a0783fc08b
Source noteuspto-grants-2012_06