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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [4-(3,3,4,4,5,5,6,6,6-Nonafluorohexyl)phenyl]methanol | HCID 16211129 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(3,3,4,4,5,5,6,6,6-Nonafluorohexyl)benzaldehyde | HCID 86613439 | 40.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737145B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1caabcd9cc0449b996621bb6bb02f26a |
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| Source note | uspto-grants-2010_06 |
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