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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17062Generated: October 29, 2026

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

https://huagongshe.com/reaction/17062

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 numberUS07737295B2
Source datasetuspto-grants-2010_06
ORD IDord-ee6070e3ae2143b68083edc55242dab9
Source noteuspto-grants-2010_06