HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451282Generated: October 25, 2026
Dimethyl Sulfoxide → 2-[Methyl(phenylmethyl)amino]acetaldehyde
https://huagongshe.com/reaction/451282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | N-Benzyl-N-methylethanolamine | HCID 66876 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sulfur trioxide-pyridine | HCID 168533 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[Methyl(phenylmethyl)amino]acetaldehyde | HCID 20644698 | — |
Reaction Steps
To a 3-necked 2-L flask was added N-benzyl-N-methylethanolamine (30.5 g, 0.182 mol), DCM (0.5 L), DIPEA (95 mL, 0.546 mol) and DMSO (41 mL, 0.728 mol). Using an ice bath, the mixture was cooled to about −10° C. and sulfur trioxide pyridine-complex (87 g, 0.546 mol) was added in 4 portions over 5 minute intervals. The reaction was stirred at −10° C. for 2 hours. Before removing the ice-bath, the reaction was quenched by adding water (0.5 L). The aqueous layer was separated and the organic layer was washed with water (0.5 L) and brine (0.5 L) and then dried over magnesium sulfate and filtered to provide the title compound which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08487107B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-e05f3d58ae1f430cbb111648208e408a |
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| Source note | uspto-grants-2013_07 |
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