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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Phytol | HCID 5280435 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,7,11,15-Tetramethylhexadec-2-enal | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703922B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e372cf8b45cf45038dfb2617d4e1f4b5 |
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| Source note | uspto-grants-2014_04 |
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