Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16478Generated: October 29, 2026

Dimethyl Sulfoxide → 4-(3,3,4,4,5,5,6,6,6-Nonafluorohexyl)benzaldehyde

https://huagongshe.com/reaction/16478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactant[4-(3,3,4,4,5,5,6,6,6-Nonafluorohexyl)phenyl]methanolHCID 16211129—
SolventDichloromethaneHCID 6344—
Product4-(3,3,4,4,5,5,6,6,6-Nonafluorohexyl)benzaldehydeHCID 8661343940.8%

Reaction Steps

To a solution of oxalyl chloride (80.2 μL, 0.93 mmol) in dichloromethane (8 mL) at −78° C., dimethyl sulfoxide (132.2 μL, 1.86 mmol) was added dropwise. After 15 minutes, 4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)benzenemethanol (300 mg, 0.85 mmol) was added. After 30 minutes, triethylamine (590 μL, 4.23 mmol) was added. The reaction was then allowed to warm to room temperature. Saturated sodium bicarbonate solution was added. The mixture was extracted with dichloromethane. The organic layer was washed with brine, dried over sodium sulfate, and concentrated under reduced pressure. Flash chromatography gave 122 mg of 4-(3,3,4,4,5,5,6,6,6-nonafluorohexyl)benzaldehyde; 1H NMR (300 MHz, CDCl3) δ 10.00 (s, 1H), 7.85 (d, 2H), 7.40 (d, 2H), 3.01 (m, 2H), 2.41 (m, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737145B2
Source datasetuspto-grants-2010_06
ORD IDord-1caabcd9cc0449b996621bb6bb02f26a
Source noteuspto-grants-2010_06