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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 892853Generated: October 30, 2026

Dimethyl Sulfoxide → o-Phenoxybenzaldehyde

https://huagongshe.com/reaction/892853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
Reactant2-Phenoxybenzyl alcoholHCID 3660111—
SolventDichloromethaneHCID 6344—
Producto-PhenoxybenzaldehydeHCID 88060—

Reaction Steps

To a solution of oxalyl chloride (6.82 g, 53.71 mmol) in CH2Cl2 (250 mL) at -78° C., was added dimethylsulfoxide (8.76 g, 112.1 mmol) dropwise. The mixture was stirred for 5 mins. A solution of crude 2-phenoxybenzyl alcohol from above in CH2Cl2 (20 mL) was added dropwise. Upon completion of addition, the reaction was stirred for 20 mins at -78∞C. Triethylamine (23.58 g, 233.5 mmol) was then added dropwise. The cooling bath was removed and the reaction allowed to warm to room temperature It was then diluted with brine (250 mL). The layers were separated and the aqueous was extracted with CH2Cl2 (2×250 mL). The organics were combined, dried with MgSO4 and concentrated. The resulting residue was chromatographed (silica gel, ether:hexanes, 20:80) to afford 7.65 g (83% over the two steps) of 2-phenoxybenzaldehyde as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05120752
Source datasetuspto-grants-1992_06
ORD IDord-0943b35bcadb4d43b99740eeea41394b
Source noteuspto-grants-1992_06