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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369292Generated: November 2, 2026

Dimethyl Sulfoxide → 3,7,11,15-Tetramethylhexadec-2-enal

https://huagongshe.com/reaction/2369292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantPhytolHCID 5280435—
SolventDichloromethaneHCID 6344—
Product3,7,11,15-Tetramethylhexadec-2-enalHCID 54256191—

Reaction Steps

Under a nitrogen atmosphere, 17.4 mL (202 mmol) of oxalyl chloride was dissolved in methylene chloride (300 mL). 36 mL (0.51 mol) of dimethyl sulfoxide was slowly added dropwise to the mixture at −78° C. After the mixture was stirred for 15 min, 50 g (0.17 mol) of phytol was added, followed by stirring for 1 hour at the same temperature. After addition of 94 mL (0.68 mol) of triethylamine, the reaction mixture was allowed to warm up to room temperature. The mixture was concentrated with methylene chloride, and the residue was diluted with diethylether, and the solution was washed saturated brine, and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated to obtain 3,7,11,15-tetramethylhexadec-2-en-1-al as a crude product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703922B2
Source datasetuspto-grants-2014_04
ORD IDord-e372cf8b45cf45038dfb2617d4e1f4b5
Source noteuspto-grants-2014_04