Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550233Generated: October 29, 2026

Dimethyl Sulfoxide → 4-Bromonaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/550233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 21906498HCID 21906498—
Reactant874357-17-2HCID 59869315—
SolventDichloromethaneHCID 6344—
Product4-Bromonaphthalene-2-carbaldehydeHCID 5433812878%

Reaction Conditions

Temperature-45 °C

Reaction Steps

Under a nitrogen atmosphere, an oxalyl chloride methylene chloride solution (2.0 M, 4.88 ml) was diluted with methylene chloride (40 ml), and dimethyl sulfoxide (0.9 ml, 12.7 mmol) was added dropwise thereto at −78° C. To this solution, a solution of (4-bromonaphthalene-2-yl)-methanol (1.15 g, 4.88 mmol) as synthesized according to a document [J. Med. Chem., 37, 2485 (1993)] in methylene chloride (10 ml) was added dropwise over 10 minutes. This reaction mixture was stirred at −78° C. for 15 minutes and −45° C. for one hour, and then triethylamine (4.0 ml, 29.3 mmol) was added dropwise thereto and stirred at 0° C. for 30 minutes. To the reaction solution, a saturated ammonium chloride aqueous solution was added and the resulting solution was extracted with methylene chloride. The organic layer was washed with water and a saturated sodium chloride aqueous solution, and dried with sodium sulfate. After filtration, the solvent was distilled under reduced pressure, and the obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:20)] to obtain the title compound (890 mg, 78%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943748B2
Source datasetuspto-grants-2011_05
ORD IDord-18e6034387304741bbd97e86c968b6a2
Source noteuspto-grants-2011_05