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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217504Generated: October 25, 2026

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

https://huagongshe.com/reaction/217504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantTriacetoxyperiodinaneHCID 159087—
Reactant[3-Bromo-5-(trifluoromethyl)phenyl]methanolHCID 29919767—
SolventDichloromethaneHCID 6344—
Product3-Bromo-5-(trifluoromethyl)benzaldehydeHCID 16115438—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of [3-bromo-5-(trifluoromethyl)phenyl]methanol (409 mg, 1.61 mmol) in CH2Cl2 (25 mL) was cooled to 0° C. and then Dess-Martin periodinane (1.02 g, 2.41 mmol) was added. The reaction was stirred at 0° C. for 30 minutes and then warmed to room temperature. After stirring at room temperature for thirty minutes, the reaction was poured into 1N NaOH (25 mL). The mixture was extracted with EtOAc (100 mL), and the organic extracts were washed with 1N NaOH (25 mL), then brine (25 mL), dried over Na2SO4, filtered, and concentrated. Purification by flash chromatography with 25% EtOAc/hexanes afforded 3-bromo-5-(trifluoromethyl)benzaldehyde. Rf=0.60 (25% EtOAc/hexanes). 1H NMR (CDCl3, 500 MHz) δ 10.02 (s, 1H), 8.20 (s, 1H), 8.07 (s, 1H), 8.02 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193365B2
Source datasetuspto-grants-2012_06
ORD IDord-c8db1d8fd8d745c88b07a88109cc08e0
Source noteuspto-grants-2012_06