Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994521Generated: October 29, 2026

Hydrochloric Acid → 2-Iodo-5-(trifluoromethyl)benzaldehyde

https://huagongshe.com/reaction/1994521

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantDiisobutylaluminum hydrideHCID 14487—
Reactant2-Iodo-5-(trifluoromethyl)benzonitrileHCID 53363644—
SolventDichloromethaneHCID 6344—
Product2-Iodo-5-(trifluoromethyl)benzaldehydeHCID 71650906—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-iodo-5-(trifluoromethyl)benzonitrile (EXAMPLE 2, 42 g) in CH2Cl2 (300 mL) at −78° C. was added a solution of DIBAL in CH2Cl2 (175 mL, 1M) over 30 minutes. A precipitate formed. The reaction was warmed to 0° C. An additional 25 mL of the DIBAL solution was added dropwise over 30 minutes. The reaction was poured into 200 mL 2N aqueous HCl, diluted with ether and stirred 1 hour. TLC analysis indicates imine still present and an additional 100 mL 2N aqueous was added and the reaction stirred overnight. Imine was still present by TLC analysis and 200 mL 2N aqueous HCl was added and the mixture stirred 2 hours. The layers were separated and the aqueous layer back extracted with ether. The ether extracts were combined, washed with brine, dried over anhydrous MgSO4, filtered and concentrated. The product was purified by silica gel chromatography eluting with 95:5 hexanes/EtOAc to give 2-Iodo-5-(trifluoromethyl)benzaldehyde as a white solid. 1H NMR (500 MHz, CDCl3): δ 10.00 (s, 1H), 8.12 (s, 1H), 8.11 (d, J=8 Hz, 1H), 7.53 (dd, J=2 Hz, 8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652049B2
Source datasetuspto-grants-2010_01
ORD IDord-bffa277419db474fb4ad236cc8da4217
Source noteuspto-grants-2010_01