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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880568Generated: November 4, 2026

Dimethyl Sulfoxide → 4-Bromo-4'-(trifluoromethoxy)biphenyl-3-carbaldehyde

https://huagongshe.com/reaction/1880568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant[4-Bromo-4'-(trifluoromethoxy)biphenyl-3-yl]methanolHCID 67485623—
SolventDichloromethaneHCID 6344—
Product4-Bromo-4'-(trifluoromethoxy)biphenyl-3-carbaldehydeHCID 86621224—

Reaction Steps

DMSO (0.69 mL, 9.72 mmol) was added dropwise to oxalyl chloride (0.42 mL, 4.86 mmol) in 4 mL DCM at −78° C. After 20 minutes a DCM solution (6 mL) of the intermediate from Step C (1.2 g, 3.47 mmol) was added dropwise. After stirring for 15 minutes at −78° C. triethylamine (2.42 mL, 17.35 mmol) was added. The reaction mixture was then allowed to warm to room temperature. The solution was partitioned between aqueous saturated NH4Cl and DCM. The organic phase was washed with water, brine, dried over Na2SO4, filtered and concentrated. The residue was purified by silica gel chromatography using a hexanes/ethyl acetate gradient to give the title compound. 1H NMR (500 MHz, CDCl3): δ 10.43 (s, 1H); 8.12 (d, J=2.4 Hz, 1H); 7.75 (d, J=8.6 Hz, 1H); 7.67-7.65 (m, 1H); 7.63 (d, J=8.5 Hz, 2H); 7.34 (d, J=8.5 Hz, 2H). LCMS1 4.09 min. (M+H)=345

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318760B2
Source datasetuspto-grants-2012_11
ORD IDord-abe076a363ca43a8a40e59bf3be8bd92
Source noteuspto-grants-2012_11